<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
    <channel>
        <title>Human Pathology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Human Pathology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Human+Pathology&t=Human+Pathology&s=Search&f=source]]></link>
        <lastBuildDate>Thu, 09 Feb 2012 00:42:12 +0100</lastBuildDate>
        <item>
            <title>On being a pathologist—passing on the torch of knowledge</title>
            <link>http://www.medworm.com/index.php?rid=5611983&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003662%2Fabstract%3Frss%3Dyes</link>
            <description>Ours was a family that valued education. My father, Herman Moe Roth, was an engineer and physicist. Before marriage, my mother, Blanche Brown, was a high school English teacher in Canadian, Oklahoma, a small rural town in the southeastern part of the state. She had studied at Washington University in St. Louis for a year and then completed her education at the University of Oklahoma in Norman. My father obtained his undergraduate degree in electrical engineering from the University of Virginia in Charlottesville. He earned his PhD in astrophysics at the Mendenhall Laboratory of Physics of Ohio State University in Columbus during the great depression. He was the only surviving boy among 7 children and used to joke that he got the education and his sisters each got a dowry. Before World War ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611983</comments>
            <pubDate>Sat, 21 Jan 2012 05:03:59 +0100</pubDate>
            <guid isPermaLink="false">5611983</guid>        </item>
        <item>
            <title>In This Issue</title>
            <link>http://www.medworm.com/index.php?rid=5611981&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711005077%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611981</comments>
            <pubDate>Sat, 21 Jan 2012 05:03:59 +0100</pubDate>
            <guid isPermaLink="false">5611981</guid>        </item>
        <item>
            <title>Table of Contents</title>
            <link>http://www.medworm.com/index.php?rid=5611980&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711005053%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611980</comments>
            <pubDate>Sat, 21 Jan 2012 05:03:59 +0100</pubDate>
            <guid isPermaLink="false">5611980</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=5611979&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711005065%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611979</comments>
            <pubDate>Sat, 21 Jan 2012 05:03:59 +0100</pubDate>
            <guid isPermaLink="false">5611979</guid>        </item>
        <item>
            <title>Editorial Board</title>
            <link>http://www.medworm.com/index.php?rid=5611978&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711005041%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611978</comments>
            <pubDate>Sat, 21 Jan 2012 05:03:59 +0100</pubDate>
            <guid isPermaLink="false">5611978</guid>        </item>
        <item>
            <title>Masthead</title>
            <link>http://www.medworm.com/index.php?rid=5611977&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100503X%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611977</comments>
            <pubDate>Sat, 21 Jan 2012 05:03:59 +0100</pubDate>
            <guid isPermaLink="false">5611977</guid>        </item>
        <item>
            <title>Necrosis assessment in renal carcinoma—reply</title>
            <link>http://www.medworm.com/index.php?rid=5496823&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003820%2Fabstract%3Frss%3Dyes</link>
            <description>We thank de Bazelaire et al for their interest in our article and appreciate the opportunity to discuss the role of tumor necrosis in renal cell carcinoma.  Tumor necrosis is often present in renal cell carcinomas. It is generally believed that tumor necrosis occurs when the blood supply cannot meet a tumor's rapid growth, reflecting aggressive biologic behavior. Several studies have found that the presence of tumor necrosis in renal cell carcinoma is closely associated with high tumor stage and poor prognosis . However, there is also conflicting evidence on whether tumor necrosis can provide any additional prognostic information beyond that of tumor grade and stage. Recent studies have found that the extent of tumor necrosis may provide more accurate prognostic information than simple pre...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496823</comments>
            <pubDate>Tue, 13 Dec 2011 18:20:43 +0100</pubDate>
            <guid isPermaLink="false">5496823</guid>        </item>
        <item>
            <title>Necrosis assessment in renal carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5496822&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003819%2Fabstract%3Frss%3Dyes</link>
            <description>We have read with interest the article by Dr Si et al reporting the clinical and pathologic features of 14 renal small cell carcinoma from 2 institutions. The tumors had a mean size of 7.1 cm and were extremely aggressive, with perinephric adipose tissue invasion at the time of diagnosis in 13 of the 14 patients. Interestingly, tumor necrosis was observed in all cases and ranged from 10% to 50% of the tumor area. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496822</comments>
            <pubDate>Tue, 13 Dec 2011 18:20:43 +0100</pubDate>
            <guid isPermaLink="false">5496822</guid>        </item>
        <item>
            <title>In This Issue</title>
            <link>http://www.medworm.com/index.php?rid=5496802&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004424%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496802</comments>
            <pubDate>Tue, 13 Dec 2011 18:20:43 +0100</pubDate>
            <guid isPermaLink="false">5496802</guid>        </item>
        <item>
            <title>Table of Contents</title>
            <link>http://www.medworm.com/index.php?rid=5496801&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004400%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496801</comments>
            <pubDate>Tue, 13 Dec 2011 18:20:43 +0100</pubDate>
            <guid isPermaLink="false">5496801</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=5496800&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004412%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496800</comments>
            <pubDate>Tue, 13 Dec 2011 18:20:43 +0100</pubDate>
            <guid isPermaLink="false">5496800</guid>        </item>
        <item>
            <title>Editorial Board</title>
            <link>http://www.medworm.com/index.php?rid=5496799&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004394%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496799</comments>
            <pubDate>Tue, 13 Dec 2011 18:20:43 +0100</pubDate>
            <guid isPermaLink="false">5496799</guid>        </item>
        <item>
            <title>Masthead</title>
            <link>http://www.medworm.com/index.php?rid=5496798&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004382%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496798</comments>
            <pubDate>Tue, 13 Dec 2011 18:20:43 +0100</pubDate>
            <guid isPermaLink="false">5496798</guid>        </item>
        <item>
            <title>Erythroid proliferations in myeloid neoplasms</title>
            <link>http://www.medworm.com/index.php?rid=5611982&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003443%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Prominent erythroid proliferations (in which erythroid elements comprise ≥50% of total bone marrow cells) can be seen in various hematopoietic stem cell neoplasms. The myeloproliferative neoplasm polycythemia vera exhibits effective, overexuberant erythropoiesis resulting in an increased red blood cell mass; in contrast, most other diseases characterized by erythroid predominance exhibit ineffective hemopoiesis. The latter include acute erythroid leukemia (erythroid-myeloid and pure erythroid leukemia subtypes) as well as some cases of myelodysplastic syndromes, acute myeloid leukemia with myelodysplasia-related changes, and therapy-related myeloid neoplasms. Some nonneoplastic reactive conditions may also manifest a striking bone marrow erythroid predominance. In this article, ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611982</comments>
            <pubDate>Mon, 12 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611982</guid>        </item>
        <item>
            <title>Acknowledgment of reviewers</title>
            <link>http://www.medworm.com/index.php?rid=5402052&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004011%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402052</comments>
            <pubDate>Sun, 13 Nov 2011 17:11:16 +0100</pubDate>
            <guid isPermaLink="false">5402052</guid>        </item>
        <item>
            <title>In this Issue</title>
            <link>http://www.medworm.com/index.php?rid=5402021&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004242%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402021</comments>
            <pubDate>Sun, 13 Nov 2011 17:11:16 +0100</pubDate>
            <guid isPermaLink="false">5402021</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=5402020&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004230%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402020</comments>
            <pubDate>Sun, 13 Nov 2011 17:11:16 +0100</pubDate>
            <guid isPermaLink="false">5402020</guid>        </item>
        <item>
            <title>Contents</title>
            <link>http://www.medworm.com/index.php?rid=5402019&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004229%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402019</comments>
            <pubDate>Sun, 13 Nov 2011 17:11:16 +0100</pubDate>
            <guid isPermaLink="false">5402019</guid>        </item>
        <item>
            <title>Editorial Board</title>
            <link>http://www.medworm.com/index.php?rid=5402018&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004217%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402018</comments>
            <pubDate>Sun, 13 Nov 2011 17:11:16 +0100</pubDate>
            <guid isPermaLink="false">5402018</guid>        </item>
        <item>
            <title>Masthead</title>
            <link>http://www.medworm.com/index.php?rid=5402017&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711004205%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402017</comments>
            <pubDate>Sun, 13 Nov 2011 17:11:16 +0100</pubDate>
            <guid isPermaLink="false">5402017</guid>        </item>
        <item>
            <title>In this Issue - November 2011</title>
            <link>http://www.medworm.com/index.php?rid=5325900&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003935%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325900</comments>
            <pubDate>Wed, 19 Oct 2011 03:38:58 +0100</pubDate>
            <guid isPermaLink="false">5325900</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=5325899&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003923%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325899</comments>
            <pubDate>Wed, 19 Oct 2011 03:38:58 +0100</pubDate>
            <guid isPermaLink="false">5325899</guid>        </item>
        <item>
            <title>Contents</title>
            <link>http://www.medworm.com/index.php?rid=5325898&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003911%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325898</comments>
            <pubDate>Wed, 19 Oct 2011 03:38:58 +0100</pubDate>
            <guid isPermaLink="false">5325898</guid>        </item>
        <item>
            <title>Editorial Board</title>
            <link>http://www.medworm.com/index.php?rid=5325897&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100390X%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325897</comments>
            <pubDate>Wed, 19 Oct 2011 03:38:58 +0100</pubDate>
            <guid isPermaLink="false">5325897</guid>        </item>
        <item>
            <title>Masthead</title>
            <link>http://www.medworm.com/index.php?rid=5325896&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003893%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325896</comments>
            <pubDate>Wed, 19 Oct 2011 03:38:58 +0100</pubDate>
            <guid isPermaLink="false">5325896</guid>        </item>
        <item>
            <title>In This Issue</title>
            <link>http://www.medworm.com/index.php?rid=5263396&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003509%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263396</comments>
            <pubDate>Thu, 29 Sep 2011 18:16:15 +0100</pubDate>
            <guid isPermaLink="false">5263396</guid>        </item>
        <item>
            <title>Table of Contents</title>
            <link>http://www.medworm.com/index.php?rid=5263395&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003480%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263395</comments>
            <pubDate>Thu, 29 Sep 2011 18:16:15 +0100</pubDate>
            <guid isPermaLink="false">5263395</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=5263394&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003492%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263394</comments>
            <pubDate>Thu, 29 Sep 2011 18:16:15 +0100</pubDate>
            <guid isPermaLink="false">5263394</guid>        </item>
        <item>
            <title>Editorial board</title>
            <link>http://www.medworm.com/index.php?rid=5263393&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003479%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263393</comments>
            <pubDate>Thu, 29 Sep 2011 18:16:15 +0100</pubDate>
            <guid isPermaLink="false">5263393</guid>        </item>
        <item>
            <title>Masthead</title>
            <link>http://www.medworm.com/index.php?rid=5263392&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003467%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263392</comments>
            <pubDate>Thu, 29 Sep 2011 18:16:15 +0100</pubDate>
            <guid isPermaLink="false">5263392</guid>        </item>
        <item>
            <title>---</title>
            <link>http://www.medworm.com/index.php?rid=5402051&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003145%2Fabstract%3Frss%3Dyes</link>
            <description>This is an excellent book that deals with recent advances in Lung Cancer, covering this subject under six sections – Overview of lung cancer, Histopathology, Imaging, Molecular pathology, Staging and Preneoplastic and preinvasive lesions. Different chapters in each of these six sections further elaborate on individual topics under consideration with smooth transitions, incorporating the current state of knowledge. Integrating the sections of Imaging, Molecular Pathology and Staging in this book, emphasizes the multimodality approach that is currently used in treating lung cancer. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402051</comments>
            <pubDate>Wed, 14 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402051</guid>        </item>
        <item>
            <title>High nuclear protein kinase Cθ expression may correlate with disease recurrence and poor survival in oral squamous cell carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5611997&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002103%2Fabstract%3Frss%3Dyes</link>
            <description>This study examined the expression of protein kinase Cθ and assessed its significance in patients with oral squamous cell carcinoma. Immunohistochemical staining was carried out to investigate the expression of protein kinase Cθ in 59 cases of oral squamous cell carcinoma. The results were correlated with clinical characteristics and outcome of patients. Diffuse cytoplasmic protein kinase Cθ was identified in 53 (89.8%) of the 59 oral squamous cell carcinoma cases, and the expression was not statistically associated with any clinicopathologic parameter. Twenty (40.7%) of the 59 oral squamous cell carcinoma cases exhibited nuclear expression of protein kinase Cθ with different grade of intensity. χ2 analysis indicated that high nuclear protein kinase Cθ expression correlated significa...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611997</comments>
            <pubDate>Tue, 16 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611997</guid>        </item>
        <item>
            <title>Liver hemangiomas and elevated serum α-fetoprotein: unsolved questions—reply</title>
            <link>http://www.medworm.com/index.php?rid=5121515&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002401%2Fabstract%3Frss%3Dyes</link>
            <description>Thank you for allowing us the opportunity to respond to the letter to the editor submitted by Bell et al in response to our article in this journal.  We appreciate and agree with the points regarding the view that use of the term liver hemangioma minimizes the chance of confusion with other adult endothelial tumors more so than does our use of “infantile hemagioendothelioma (IHE)”of the liver . IHE was adopted in the World Health Organization (WHO) classification of tumors in 2000 . “Hemangioma of infancy” has been adopted by the WHO for the skin , whereas IHE has been reserved for the liver because of the presence of histologically more aggressive type of IHE and occasional reports of transformation of hepatic IHE to angiosarcoma . However, the terminology and concept of this enti...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121515</comments>
            <pubDate>Fri, 12 Aug 2011 23:56:09 +0100</pubDate>
            <guid isPermaLink="false">5121515</guid>        </item>
        <item>
            <title>Liver hemangiomas and elevated serum α-fetoprotein: unsolved questions</title>
            <link>http://www.medworm.com/index.php?rid=5121514&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002395%2Fabstract%3Frss%3Dyes</link>
            <description>We read with interest the report by Kim and colleagues in which the authors credibly explained the phenomenon of elevated serum α-fetoprotein (AFP) in 2 infants with hepatic infantile hemangioma. The source of AFP, as demonstrated immunohistochemically, was the hepatocytes located near or entrapped within the tumor. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121514</comments>
            <pubDate>Fri, 12 Aug 2011 23:56:09 +0100</pubDate>
            <guid isPermaLink="false">5121514</guid>        </item>
        <item>
            <title>S-100P, von Hippel-Lindau gene product, and IMP3 serve as a useful immunohistochemical panel in the diagnosis of adenocarcinoma on endoscopic bile duct biopsy—reply</title>
            <link>http://www.medworm.com/index.php?rid=5121513&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002218%2Fabstract%3Frss%3Dyes</link>
            <description>We would like to thank Drs Riener and Kristiansen for their interest in our article and would like to apologize for our inadvertent negligence of not citing their excellent study . We were pleased to learn that, of their 115 cases of surgically resected bile duct carcinomas, 67 (58.3%) showed strong IMP3 (the insulinlike growth factor-II mRNA binding protein-3) immunoreactivity. In contrast, bile ducts with normal histology, acute inflammation, or reactive epithelial changes were negative or only weakly positive for IMP3. These data reaffirm our observations that IMP3 is a useful diagnostic immunomarker that can aid in the distinction between benign and malignant biliary epithelial lesions. Although our study was focused on endoscopic biopsies of the extrahepatic bile ducts, the cases exam...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121513</comments>
            <pubDate>Fri, 12 Aug 2011 23:56:08 +0100</pubDate>
            <guid isPermaLink="false">5121513</guid>        </item>
        <item>
            <title>In This Issue September 2011</title>
            <link>http://www.medworm.com/index.php?rid=5121490&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003030%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121490</comments>
            <pubDate>Fri, 12 Aug 2011 23:55:55 +0100</pubDate>
            <guid isPermaLink="false">5121490</guid>        </item>
        <item>
            <title>Table of Contents</title>
            <link>http://www.medworm.com/index.php?rid=5121489&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003017%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121489</comments>
            <pubDate>Fri, 12 Aug 2011 23:55:55 +0100</pubDate>
            <guid isPermaLink="false">5121489</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=5121488&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003029%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121488</comments>
            <pubDate>Fri, 12 Aug 2011 23:55:55 +0100</pubDate>
            <guid isPermaLink="false">5121488</guid>        </item>
        <item>
            <title>Editorial Board</title>
            <link>http://www.medworm.com/index.php?rid=5121487&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711003005%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121487</comments>
            <pubDate>Fri, 12 Aug 2011 23:55:55 +0100</pubDate>
            <guid isPermaLink="false">5121487</guid>        </item>
        <item>
            <title>Masthead</title>
            <link>http://www.medworm.com/index.php?rid=5121486&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002991%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121486</comments>
            <pubDate>Fri, 12 Aug 2011 23:55:55 +0100</pubDate>
            <guid isPermaLink="false">5121486</guid>        </item>
        <item>
            <title>Cytogenetic and comparative genomic hybridization studies of an esophageal giant fibrovascular polyp: a case report</title>
            <link>http://www.medworm.com/index.php?rid=5612000&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001924%2Fabstract%3Frss%3Dyes</link>
            <description>We present the pathologic and cytogenetic findings of an 18-cm esophageal giant fibrovascular polyp in a 49-year-old woman who presented with odynophagia and dysphagia. The histologic findings are that of classic esophageal giant fibrovascular polyp as previously described in the literature. Cytogenetic study revealed an abnormal karyotype, and comparative genomic hybridization analysis showed regional amplifications of chromosomes 3 and 12 and a possible loss of 22q13.3-qter. The significance of these cytogenetic findings is unclear but may suggest a neoplastic process in the pathogenesis of esophageal giant fibrovascular polyps. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5612000</comments>
            <pubDate>Thu, 11 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5612000</guid>        </item>
        <item>
            <title>Prognostic role of metastasis tumor antigen 1 in patients with ovarian cancer: a clinical study</title>
            <link>http://www.medworm.com/index.php?rid=5611998&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002115%2Fabstract%3Frss%3Dyes</link>
            <description>In this study, we investigated the prognostic value of metastasis tumor antigen 1 expression in 81 untreated patients with ovarian cancer. The expression of metastasis tumor antigen 1 was evaluated by immunohistochemistry, and staining was analyzed in relation to clinicopathologic variables, disease-free survival, and overall survival. High expression of metastasis tumor antigen 1 was found to be associated with advanced stage (I/II versus III/IV, P = .02) and with worse response to first-line treatment (P = .03). Cases with high metastasis tumor antigen 1 expression showed a lower disease-free survival compared with cases with low expression (P = .02). In multivariate analysis of disease-free survival, metastasis tumor antigen 1 overexpression retained an independent negative prognostic r...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611998</comments>
            <pubDate>Thu, 11 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611998</guid>        </item>
        <item>
            <title>High CD10 expression predicts favorable outcome in surgically treated lymph node–positive bladder cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5611996&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002036%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: CD10 predicts survival in different cancers. The prognostic significance in bladder cancer still has to be documented. One hundred fifty lymph node–positive bladder cancer patients were treated by cystectomy and standardized pelvic lymphadenectomy in curative intent. CD10 expression was evaluated in tissue microarrays (TMAs) constructed from histopathological normal urothelium, primary tumor (tumor center and invasion front), and corresponding lymph node metastases and correlated with tumor characteristics (stage, extracapsular extension, number, and total diameter of metastases) and survival. CD10 expression was successively lost from normal urothelium to primary tumor to metastases (P &lt; .05) and decreased from the tumor center to the invasion front (P &lt; .002). High CD10 expres...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611996</comments>
            <pubDate>Thu, 11 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611996</guid>        </item>
        <item>
            <title>Folliculocentric B-cell–rich follicular dendritic cells sarcoma: a hitherto unreported morphological variant mimicking lymphoproliferative disorders</title>
            <link>http://www.medworm.com/index.php?rid=5611988&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001882%2Fabstract%3Frss%3Dyes</link>
            <description>This study further emphasizes the extreme variability of morphological presentation of FDCS and expands the spectrum of lesions showing a nodular growth pattern occurring in human lymph nodes. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611988</comments>
            <pubDate>Thu, 11 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611988</guid>        </item>
        <item>
            <title>Warty/basaloid penile intraepithelial neoplasia is more prevalent than differentiated penile intraepithelial neoplasia in nonendemic regions for penile cancer when compared with endemic areas: a comparative study between pathologic series from Paris and Paraguay</title>
            <link>http://www.medworm.com/index.php?rid=5611986&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001833%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Penile squamous cell carcinoma shows an ample geographic variation in its prevalence with regions of low (North America, Europe, Japan, and Israel) and high (Africa, Asia, and South America) incidence. However, the geographic variation in the distribution of penile intraepithelial neoplasia is not well established. The aim of the present study was to compare the distribution of in situ and invasive lesions between geographic areas with low (France) and high (Paraguay) penile cancer incidence using a series of consecutive cases. The French series included 86 cases (57 in situ and 29 in situ + invasive squamous cell carcinoma), and the Paraguayan series, 117 cases (31 in situ and 86 in situ + invasive squamous cell carcinoma). Incidence of invasive squamous cell carcinoma in the ove...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611986</comments>
            <pubDate>Thu, 11 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611986</guid>        </item>
        <item>
            <title>Indeterminate cell tumor of the spleen</title>
            <link>http://www.medworm.com/index.php?rid=5612003&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001997%2Fabstract%3Frss%3Dyes</link>
            <description>We report a case of indeterminate cell tumor arising from the spleen, a previously unreported site for indeterminate cell tumor. Histologically, the tumor showed nests, nodules, and sheets of large polygonal cells with mostly oval nuclei; open chromatin; variable nucleoli; and abundant, eosinophilic cytoplasm. Some cells possessed irregularly convoluted nuclei with nuclear grooves and granular cytoplasm, suggestive of Langerhans cells. Immunohistochemically, the tumor cells were diffusely positive for S-100 and CD1a and negative for Langerin. No Birbeck granules were found by electron microscopy. Clinical and radiologic examination showed no other organomegaly or lymphadenopathy. A diagnosis of primary indeterminate cell tumor of the spleen was rendered. To the best of our knowledge, this ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5612003</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5612003</guid>        </item>
        <item>
            <title>Sensitivity and specificity of finding of multinucleate trophoblastic giant cells in decidua in placentas from high-risk pregnancies</title>
            <link>http://www.medworm.com/index.php?rid=5611995&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002024%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, finding of multinucleate trophoblastic giant cells is not exclusively limited to uteroplacental malperfusion of preeclampsia but is also seen in other types of high-risk pregnancy and in association with other placental hypoxic lesions and patterns. Multinucleate trophoblastic giant cells most likely reflect a premature fusion of extravillous trophoblasts because of several factors, likely including also hypoxia. Being highly specific, finding the multinucleate trophoblastic giant cells is unlikely to give a false-positive result and therefore has high value in retrospectively explaining the perinatal morbidity and mortality. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611995</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611995</guid>        </item>
        <item>
            <title>Characteristics of positive surgical margins in robotic-assisted radical prostatectomy, open retropubic radical prostatectomy, and laparoscopic radical prostatectomy: a comparative histopathologic study from a single academic center</title>
            <link>http://www.medworm.com/index.php?rid=5611994&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002000%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Studies detailing differences in positive surgical margin among open retropubic radical prostatectomy, laparoscopic radical prostatectomy, and robotic-assisted laparoscopic radical prostatectomy are lacking. A retrospective review of all prostatectomies with positive surgical margin performed at our center in 2007 disclosed 99 cases, 6 (5%) of which were reinterpreted cases as having negative margins. Ninety-three cases were, therefore, included, corresponding to 37 retropubic radical prostatectomies, 19 laparoscopic radical prostatectomies, and 37 robotic-assisted laparoscopic radical prostatectomies. The relationship of positive surgical margin characteristics to clinicopathologic parameters and biochemical recurrence was assessed. The most commonly found positive surgical margi...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611994</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611994</guid>        </item>
        <item>
            <title>Vulvovaginal myofibroblastoma: expanding the morphological and immunohistochemical spectrum. A clinicopathologic study of 10 cases</title>
            <link>http://www.medworm.com/index.php?rid=5611993&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001985%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: We analyzed the clinicopathologic features of 10 cases of vulvovaginal myofibroblastoma to widen its morphological and immunohistochemical spectrum. Most tumors (8/10 cases) were located in the vagina. The patients' age ranged from 44 to 77 years, and tumor size ranged from 0.4 to 3 cm. Histologically, 5 tumors had the characteristics of vulvovaginal myofibroblastoma. In addition, we identified 3 cases composed of spindle-shaped cells arranged in short fascicles with intervening thick collagen bands, closely reminiscent of mammary myofibroblastoma. Notably, 1 case resembled Sertoli cell tumor, sclerosing type, because of its predominant cord-like arrangement. In another case, there were highly cellular areas composed of uniform-packed, rounded cells that, at low magnification, loo...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611993</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611993</guid>        </item>
        <item>
            <title>Dysplastic lesions in inflammatory bowel disease show increased positivity for the stem cell marker aldehyde dehydrogenase</title>
            <link>http://www.medworm.com/index.php?rid=5611992&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001973%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: The chronic inflammatory state in patients with inflammatory bowel disease places them at a substantially elevated risk for developing colorectal carcinoma. Moreover, distinguishing an inflammatory phenotype from dysplasia in inflammatory bowel disease can be difficult and has significant patient management implications. To this end, we studied the expression of the cancer stem cell marker aldehyde dehydrogenase to determine whether expression is increased in dysplastic lesions arising in inflammatory bowel disease. We studied 54 patients with inflammatory bowel disease who underwent surgical resection. Of the 54 patients, 13 exhibited high-grade dysplasia or adenocarcinoma, 19 exhibited low-grade dysplasia, and 22 displayed only inflammatory atypia. Staining for aldehyde dehydrog...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611992</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611992</guid>        </item>
        <item>
            <title>Regulatory role of p53 in cancer metabolism via SCO2 and TIGAR in human breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5611990&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001912%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Cancer cells show a higher rate of anaerobic respiration than normal cells. The exact mechanisms for this higher glycolysis rate in cancer cells remain to be elucidated. The results of recent studies have indicated that p53, the most commonly mutated tumor suppressor gene, may have important functions in the regulation of energy-generating metabolic pathways that switch from oxidative phosphorylation to glycolysis via the synthesis of cytochrome c oxidase 2 (SCO2), p53-transactivated TP53-induced glycolysis (TIGAR), and apoptosis regulator. We evaluated the expression of p53, SCO2, TIGAR, and COX in 113 cases of invasive breast cancer using immunohistochemistry. A high expression of p53, SCO2, TIGAR, and COX was noted in 27.5% (31 cases), 84.1% (95 cases), 74.3% (84 cases), and 73...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611990</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611990</guid>        </item>
        <item>
            <title>Anal duct carcinoma: a report of 5 cases</title>
            <link>http://www.medworm.com/index.php?rid=5611989&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001894%2Fabstract%3Frss%3Dyes</link>
            <description>We describe the clinicopathologic characteristics and follow-up of 5 cases of ADC. Four definitive cases had tissue available for immunohistochemistry (IHC; CK7, CK20, prostate-specific antigen [PSA], estrogen/progesterone receptors [ER/PR], and p16) and in situ hybridization (ISH) for high-risk human papillomavirus (HR-HPV); a fifth case, with a history of ADC, had limited tissue for immunolabeling with only CK7, CK20, and p16. The mean patient age was 69.8 years. All 5 cases were CK7-positive and p16-negative. Four of 5 cases were CK20-negative. All cases with sufficient tissue (4/4) were negative for HR-HPV by ISH, PSA-negative (men), and ER/PR-negative (women). Four of 5 patients had previous malignancies, and in all 4 cases with sufficient tissue, metastasis was excluded with IHC. Of ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611989</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611989</guid>        </item>
        <item>
            <title>Metallothionein expression in colorectal cancer: relevance of different isoforms for tumor progression and patient survival</title>
            <link>http://www.medworm.com/index.php?rid=5611987&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001845%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Metallothioneins are a family of small, cysteine-rich proteins with many functions. Immunohistochemical evaluation of all metallothionein 1 + 2 isoforms in colorectal tumors has demonstrated an important down-regulation compared with normal tissue, although its prognostic significance is unclear. Moreover, the contribution of individual isoforms to overall metallothionein down-regulation is not known. To address these important issues, we analyzed the messenger RNA expression levels of all functional metallothionein 1 + 2 isoforms by quantitative reverse transcription polymerase chain reaction in 22 pairs of normal and tumor-microdissected epithelia and correlated these to the overall immunohistochemical protein expression. Our results showed that 5 isoforms (MT1G, 1E, 1F, 1H, and...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611987</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611987</guid>        </item>
        <item>
            <title>Fluorescence in situ hybridization mapping of esophagectomy specimens from patients with Barrett's esophagus with high-grade dysplasia or adenocarcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5611984&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001870%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: The progression of intestinal metaplasia to esophageal adenocarcinoma in patients with Barrett's esophagus is partly driven by chromosomal alterations that activate oncogenes and inactivate tumor suppressor genes. The goal of this study was to determine how alterations of 4 frequently affected genes correlate with the range of histopathologic lesions observed in resected esophagi of patients with Barrett's esophagus. Fluorescence in situ hybridization was used to assess 83 tissue sections from 10 Barrett's esophagus esophagogastrectomy specimens for chromosomal alterations of 8q24 (MYC), 9p21 (CDKN2A; alias P16), 17q12 (ERBB2), and 20q13.2 (ZNF217). Histologic lesions assessed included gastric metaplasia (n = 8), intestinal metaplasia (n = 43), low-grade dysplasia (n = 28), high-g...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611984</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611984</guid>        </item>
        <item>
            <title>High-grade papillary urothelial carcinoma of the urinary tract: a clinicopathologic analysis of a post–World Health Organization/International Society of Urological Pathology classification cohort from a single academic center</title>
            <link>http://www.medworm.com/index.php?rid=5496816&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001821%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, recurrence, progression, and cancer-specific mortality rates were 36.5%, 40%, and 15%, respectively. All the patients who died of cancer had a history of tumor progression. Patients with recurrences showed similar outcomes to those with no recurrence. Tumor size was strongly associated with tumor progression and cancer-specific survival, whereas clinical stage was significantly associated with outcome in the progression group. In light of the high recurrence and progression rates of high-grade papillary urothelial carcinoma, strict clinical surveillance aimed to detect early recurrent lesions, especially in patients with larger tumors, is warranted. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496816</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496816</guid>        </item>
        <item>
            <title>Pediatric adrenocortical tumors: morphological diagnostic criteria and immunohistochemical expression of matrix metalloproteinase type 2 and human leucocyte-associated antigen (HLA) class II antigens: Results from the Italian Pediatric Rare Tumor (TREP) Study project</title>
            <link>http://www.medworm.com/index.php?rid=5496806&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001857%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Pediatric adrenocortical tumors are neoplasms that only rarely occur in pediatric patients. Their clinical behavior is often unpredictable, and the histologic criteria of malignancy used in adults are not always useful in children. The aim of this study was to validate the prognostic value of the pathologic criteria of Wieneke et al and to evaluate the potential prognostic expression of matrix metalloproteinase 2 and human leucocyte-associated antigen (HLA) class II antigens in a series of 20 pediatric patients affected by adrenocortical tumors, who were enrolled in the Italian Pediatric Rare Tumor (TREP) Study between 2000 and 2007. The age range was 0 to 17.5 years (mean, 7.28 years) with a male-female ratio of 1:2. The mean follow-up was 64.4 months. The histologic diagnoses we...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496806</comments>
            <pubDate>Fri, 05 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496806</guid>        </item>
        <item>
            <title>Signet ring cell tumor of the minor salivary gland exhibiting benign behavior</title>
            <link>http://www.medworm.com/index.php?rid=5612002&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001961%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Signet ring cell (SRC) carcinomas are usually aggressive malignancies, arising most frequently in the stomach and gastrointestinal tract, but also, although less often, in other organs such as the breast, bladder, and lungs. They are particularly unusual in the salivary glands, and the aim of the present study is to report a case of a tumor of the minor salivary glands of the lower lip composed largely of SRCs but which displayed benign clinical behavior. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5612002</comments>
            <pubDate>Wed, 03 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5612002</guid>        </item>
        <item>
            <title>The CIC-DUX4 fusion transcript is present in a subgroup of pediatric primitive round cell sarcomas</title>
            <link>http://www.medworm.com/index.php?rid=5611985&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001936%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Pediatric undifferentiated soft tissue sarcomas are a group of diagnostically challenging tumors. Recent studies have identified a subgroup of undifferentiated soft tissue sarcomas with primitive round to plump spindle cell morphology and a t(4;19)(q35;q13.1) translocation resulting in the expression of a CIC-DUX4 fusion transcript, including 2 tumors previously reported by our laboratory (Cancer Genet Cytogenet 2009;195:1). In the present study, reverse transcriptase polymerase chain reaction assays developed for both frozen and paraffin-based tissues were applied to a series of 19 pediatric undifferentiated soft tissue sarcomas using a combination of primer sets covering the CIC-DUX4 fusion transcript. Of the 19 undifferentiated soft tissue sarcomas, 16 had primitive round to pl...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611985</comments>
            <pubDate>Wed, 03 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611985</guid>        </item>
        <item>
            <title>Myoid gonadal stromal tumor: a distinct testicular tumor with peritubular myoid cell differentiation</title>
            <link>http://www.medworm.com/index.php?rid=5496821&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001869%2Fabstract%3Frss%3Dyes</link>
            <description>We report a distinct, primary testicular tumor with peritubular myoid cell differentiation. A 25-year-old man developed a well-circumscribed testicular tumor composed of cytologically bland spindled cells, which were strongly and diffusely positive for desmin, smooth muscle actin, muscle-specific actin, and smooth muscle myosin. In addition, S-100 was diffusely positive, and cytokeratin (CK5/6 and AE1/3) was focally positive. Calretinin, inhibin, and CD34 were all negative. This pattern of immunoreactivity was very similar to the normal adjacent peritubular myoid cells. Follow-up after radical orchiectomy showed benign behavior. We found reports of 6 similar intratesticular tumors demonstrating peritubular myoid cell–like differentiation and having favorable outcome. We believe that the ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496821</comments>
            <pubDate>Wed, 03 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496821</guid>        </item>
        <item>
            <title>Ectomesenchymoma with t(1;12)(p32;p13) evolving from embryonal rhabdomyosarcoma shows no rearrangement of ETV6</title>
            <link>http://www.medworm.com/index.php?rid=5612001&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100195X%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Ectomesenchymoma is a rare mesenchymal malignancy occurring mainly in the pediatric population. The hallmark diagnostic features are a combination of sarcoma, usually rhabdomyosarcoma (RMS) with admixed ganglion cells. The lesion arises either in soft tissues or the cranial cavity, and outcomes vary considerably. Current knowledge about the genetics and biology of ectomesenchymoma is extremely limited with only 4 published karyotypes, showing overlaps only in trisomies 2, 8, and 11. Here, we describe a case with genetic findings that, in conjunction with preexisting observations, offer some additional insights into the genetic aberrations of ectomesenchymoma. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5612001</comments>
            <pubDate>Mon, 01 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5612001</guid>        </item>
        <item>
            <title>Tumor of the heart in a young woman; a rare manifestation of Wegener granulomatosis</title>
            <link>http://www.medworm.com/index.php?rid=5611999&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001900%2Fabstract%3Frss%3Dyes</link>
            <description>We report a case of a 19-year-old woman with no prior significant medical history who presented with persistent ventricular tachycardia and a papillary muscle mass in her left ventricle which upon excision and tissue evaluation demonstrated histologic changes of Wegener granulomatosis. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611999</comments>
            <pubDate>Mon, 01 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611999</guid>        </item>
        <item>
            <title>Immunoreactivity to caspase-3, caspase-7, caspase-8, and caspase-9 forms is frequently lost in human prostate tumors</title>
            <link>http://www.medworm.com/index.php?rid=5611991&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001948%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Caspases are essential initiators and executioners of apoptosis. Changes in their expression may contribute to the development of proliferative disorders such as cancer, by altering the death-proliferation homeostatic balance. The aim of this work was to analyze the expression of a broad panel of caspases at the epithelial level in human prostate tissues to assess possible prostatic disease–related alterations. We comparatively analyzed by immunohistochemistry the expression of pro–caspase-3, pro–caspase-8, pro–caspase-9, cleaved caspase-3, cleaved caspase-8, and caspase-7, in normal and pathologic (benign hyperplasic, premalignant [high-grade intraepithelial neoplasia], and cancerous [prostate cancer]) human prostate epithelium. Expression of caspases was correlated with ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5611991</comments>
            <pubDate>Fri, 29 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5611991</guid>        </item>
        <item>
            <title>Overexpression of optic atrophy 1 protein increases cisplatin resistance via inactivation of caspase-dependent apoptosis in lung adenocarcinoma cells</title>
            <link>http://www.medworm.com/index.php?rid=5496815&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100181X%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, optic atrophy 1 is highly expressed in lung adenocarcinoma and indicates poor prognosis. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496815</comments>
            <pubDate>Thu, 28 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496815</guid>        </item>
        <item>
            <title>Erratum to “Cytogenetic and molecular aberrations in endometrial stromal tumors” (Hum Pathol 2011;42:609-617)</title>
            <link>http://www.medworm.com/index.php?rid=5263424&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002644%2Fabstract%3Frss%3Dyes</link>
            <description>The aforementioned authors have noted that reference number in their article cites the wrong reference information. The correct reference appears below. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263424</comments>
            <pubDate>Thu, 28 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5263424</guid>        </item>
        <item>
            <title>Relationship between amyloid deposition and intracellular structural changes in familial amyloidotic polyneuropathy</title>
            <link>http://www.medworm.com/index.php?rid=5496814&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100178X%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Transthyretin-related familial amyloidotic polyneuropathy is a systemic amyloidosis caused by mutations in the transthyretin gene. Extracellular deposition of amyloid is the common pathologic hallmark of amyloidoses including Alzheimer disease, AL amyloidosis, AA amyloidosis, and familial amyloidotic polyneuropathy. However, the exact relationship between amyloid deposition and cell death has not yet been clarified. To elucidate this relationship, we studied the effect of transthyretin amyloid fibrils and prefibrillar aggregates on cells by using autopsy tissues obtained from 8 patients with familial amyloidotic polyneuropathy, as well as cultured cell lines. Ultrastructural studies of amyloid-laden cardiomyocytes showed that intracellular structural changes correlated with the de...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496814</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496814</guid>        </item>
        <item>
            <title>Immunohistochemical markers of tissue injury in biopsies with transplant glomerulitis</title>
            <link>http://www.medworm.com/index.php?rid=5496811&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001626%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, glomerular injury in transplant glomerulitis appears to be mediated by complement activation and cellular cytotoxicity. Mesangial– or interstitial–von Willebrand factor identified cases with more severe microcirculation injury. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496811</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496811</guid>        </item>
        <item>
            <title>Decreased Beclin-1 expression is correlated with the growth of the primary tumor in patients with squamous cell carcinoma and adenocarcinoma of the lung</title>
            <link>http://www.medworm.com/index.php?rid=5496810&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001614%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Beclin-1 is a Bcl-2–interacting protein, and it may delay cell cycle progression and induce autophagy. The function and expression of Beclin-1 and Bcl-2 in squamous cell carcinoma and adenocarcinoma of the lung remain largely unknown. Herein, we investigated the expression of Beclin-1 and Bcl-2 in squamous cell carcinoma and adenocarcinoma of the lung. Tissue samples from 262 cases were used in this study. Immunohistochemical staining for Beclin-1 and Bcl-2 were conducted using a tissue microarray. In squamous cell carcinoma, Beclin-1 expression was strongly positive in 48 (28.6%) of 168 samples, it was moderately positive in 42 (25.0%) of 168 samples, and it was negative or weakly positive in 78 (46.4%) of 168 samples. In adenocarcinoma, Beclin-1 expression was strongly positiv...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496810</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496810</guid>        </item>
        <item>
            <title>Detection of hepatitis B virus DNA in paraffin-embedded intrahepatic and extrahepatic cholangiocarcinoma tissue in the northern Chinese population</title>
            <link>http://www.medworm.com/index.php?rid=5496809&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001584%2Fabstract%3Frss%3Dyes</link>
            <description>This study explored the importance of hepatitis B virus infection in cholangiocarcinoma pathogenesis in northern China. The clinical data of 66 patients with cholangiocarcinoma were analyzed. The hepatitis B virus gene was amplified using nested polymerase chain reaction, and the hepatitis B virus–related antigen was detected using immunohistochemistry in formalin-fixed, paraffin-embedded tissue from patients with intrahepatic cholangiocarcinoma (n = 23) and extrahepatic cholangiocarcinoma (n = 43). Hepatitis B surface antigen seropositivity was found in 52.2% (12/23) of intrahepatic cholangiocarcinoma cases and 13.9% (6/43) of extrahepatic cholangiocarcinoma cases. Hepatitis B virus DNA (X region) was detectable in 34.8% (8/23) of intrahepatic cholangiocarcinoma cases. Hepatitis B surfa...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496809</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496809</guid>        </item>
        <item>
            <title>Prognostic significance of Bcl-2 in invasive mammary carcinomas: a comparative clinicopathologic study between “triple-negative” and non–“triple-negative” tumors</title>
            <link>http://www.medworm.com/index.php?rid=5496805&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001808%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, there are major clinicopathologic differences between breast cancer phenotypes. Our results establish the value of using Bcl-2 in prognostic stratification of patients and its potential therapeutic implications in selecting patients for treatment. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496805</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496805</guid>        </item>
        <item>
            <title>Incidence of human papillomavirus in oropharyngeal squamous cell carcinomas: now and 50 years ago</title>
            <link>http://www.medworm.com/index.php?rid=5496804&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001791%2Fabstract%3Frss%3Dyes</link>
            <description>This study provides the earliest historic baseline for human papillomavirus incidence in oropharyngeal squamous cell carcinoma and may serve as a reference point for evaluating the results of human papillomavirus infection preventive measures, such as human papillomavirus vaccination. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496804</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496804</guid>        </item>
        <item>
            <title>Intraductal papillary mucinous neoplasm</title>
            <link>http://www.medworm.com/index.php?rid=5496803&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001572%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Intraductal papillary mucinous neoplasm (IPMN) is a grossly visible (≥1 cm), mucin-producing neoplasm that arises in the main pancreatic duct and/or its branches. Patients with intraductal papillary mucinous neoplasm can present with symptoms caused by obstruction of the pancreatic duct system, or they can be asymptomatic. There are 3 clinical subtypes of intraductal papillary mucinous neoplasm: main duct, branch duct, and mixed. Five histologic types of intraductal papillary mucinous neoplasm are recognized: gastric foveolar type, intestinal type, pancreatobiliary type, intraductal oncocytic papillary neoplasm, and intraductal tubulopapillary neoplasm. Noninvasive intraductal papillary mucinous neoplasms are classified into 3 grades based on the degree of cytoarchitectural atyp...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496803</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496803</guid>        </item>
        <item>
            <title>Fluorescence in situ hybridization for detection of MAML2 rearrangements in oncocytic mucoepidermoid carcinomas: utility as a diagnostic test</title>
            <link>http://www.medworm.com/index.php?rid=5402042&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001511%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Oncocytic mucoepidermoid carcinoma poses diagnostic challenge because of its histologic overlap with other oncocytic salivary gland lesions, including Warthin tumor. Although the prognostic value of the t(11;19) MECT1-MAML2 fusion gene has been established in mucoepidermoid carcinoma, its diagnostic use in discriminating oncocytic mucoepidermoid carcinoma from histologic mimics is unexplored. We evaluated the translocation status in 14 cases of oncocytic mucoepidermoid carcinoma using a MAML2-11q21 break-apart probe spanning the entire chromosome region of the MAML2 gene and correlated these findings with clinicopathologic parameters including age, sex, stage, predominant growth pattern, grade, and p63 immunostaining pattern. All oncocytic mucoepidermoid carcinomas were parotid tu...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402042</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402042</guid>        </item>
        <item>
            <title>Papillary urothelial neoplasm of low malignant potential of the urinary bladder: clinicopathologic and outcome analysis from a single academic center</title>
            <link>http://www.medworm.com/index.php?rid=5366956&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001468%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, recurrences were observed in 42% of all our patients, with a grade progression rate of 29%. None of our patients developed invasive carcinoma or died as a consequence of their disease. Considering the low but definitive risk of recurrence and grade progression, appropriate clinical follow-up of patients with primary papillary urothelial neoplasm of low malignant potential is warranted. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5366956</comments>
            <pubDate>Thu, 21 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5366956</guid>        </item>
        <item>
            <title>Intravenous leiomyomatosis of the uterus: A clinicopathologic study of 18 cases, with emphasis on early diagnosis and appropriate treatment strategies</title>
            <link>http://www.medworm.com/index.php?rid=5121494&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817710004077%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Intravenous leiomyomatosis is a rare variant of leiomyoma that could result in death. Early and accurate diagnosis and appropriate treatment strategies play a dominant role in good prognosis. Eighteen cases of Intravenous leiomyomatosis , along with clinicopathologic data, were retrieved from our database. Most of the patients who ranged in age from 33 to 54 years (median, 44 years) presented with a pelvic mass or abnormal uterine bleeding. The diagnosis was confirmed by a immunohistochemical staining for smooth muscle actin, CD34, and Ki67. Surgical exploration confirmed the presence of a uterine mass (mean size, 5.08 cm). Wormlike plugs were identified within the broad ligament in 5 cases. The tumor penetrated to the inferior vena cava in 1 case. Histologic variants were noted i...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121494</comments>
            <pubDate>Wed, 20 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5121494</guid>        </item>
        <item>
            <title>BRAFV600E mutation analysis of liquid-based preparation–processed fine needle aspiration sample improves the diagnostic rate of papillary thyroid carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5496813&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100164X%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Early detection and diagnosis of papillary thyroid carcinoma are important for successful management of patients. Liquid-based preparations (Thinprep) of fine needle aspirations from thyroid nodules are now widely used and are replacing conventional smears because residual samples can be used for ancillary tests. Detection of the BRAFV600E mutation in cytology specimens could aid in the diagnosis of papillary thyroid carcinoma. We, therefore, analyzed the cytologic features and BRAFV600E mutation status of thyroid liquid-based preparation–fine needle aspiration samples. A total of 191 histologically confirmed thyroid liquid-based preparation–fine needle aspiration specimens were selected. We analyzed cytomorphological features and BRAFV600E mutation status in both liquid-based...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496813</comments>
            <pubDate>Wed, 20 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496813</guid>        </item>
        <item>
            <title>In This Issue August 2011</title>
            <link>http://www.medworm.com/index.php?rid=5032287&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100270X%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032287</comments>
            <pubDate>Sun, 17 Jul 2011 03:16:30 +0100</pubDate>
            <guid isPermaLink="false">5032287</guid>        </item>
        <item>
            <title>Table of Contents</title>
            <link>http://www.medworm.com/index.php?rid=5032286&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002681%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032286</comments>
            <pubDate>Sun, 17 Jul 2011 03:16:30 +0100</pubDate>
            <guid isPermaLink="false">5032286</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=5032285&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002693%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032285</comments>
            <pubDate>Sun, 17 Jul 2011 03:16:30 +0100</pubDate>
            <guid isPermaLink="false">5032285</guid>        </item>
        <item>
            <title>Editorial Board</title>
            <link>http://www.medworm.com/index.php?rid=5032284&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100267X%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032284</comments>
            <pubDate>Sun, 17 Jul 2011 03:16:30 +0100</pubDate>
            <guid isPermaLink="false">5032284</guid>        </item>
        <item>
            <title>Masthead</title>
            <link>http://www.medworm.com/index.php?rid=5032283&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002668%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032283</comments>
            <pubDate>Sun, 17 Jul 2011 03:16:29 +0100</pubDate>
            <guid isPermaLink="false">5032283</guid>        </item>
        <item>
            <title>In situ follicular lymphoma with progressive transformation of the germinal centers confirmed by laser capture microdissection, IGH gene rearrangement analysis, and fluorescence in situ hybridization for t(14;18)</title>
            <link>http://www.medworm.com/index.php?rid=5496820&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001547%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: The authors report an unusual case of in situ follicular lymphoma associated with progressive transformation of the germinal centers. The patient was a 74-year-old Chinese woman with sequential lymphadenopathy in the right and left cervical regions over a period of 2 months. The first biopsy revealed in situ follicular lymphoma with progressive transformation of germinal centers, and the biopsy of the second lymph node led to a diagnosis of in situ follicular lymphoma. The immunophenotype, polymerase chain reaction amplification of the immunoglobulin heavy chain gene, and fluorescence in situ hybridization for t(14;18) were analyzed in each biopsy specimen, which showed both specimens to have t(14;18)(q32;q21) and revealed progression from polyclonality to monoclonality. These fin...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496820</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496820</guid>        </item>
        <item>
            <title>Pleomorphic adenoma arising in an incidental midline isthmic thyroid nodule: a case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5496819&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001481%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Ectopic salivary gland tissue is common in the head and neck, usually associated with lymph nodes in lateral areas. It is rarely noted in the thyroid gland. Here we report the first case of a pleomorphic adenoma presenting as a midline nodule in the isthmus of thyroid in a 66-year-old man. We propose the possibility of origin in ectopic salivary gland tissue that may have aberrantly migrated with the median anlage from the foramen cecum in the base of the tongue during embryogenesis. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496819</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496819</guid>        </item>
        <item>
            <title>In immunocompromised patients, Epstein-Barr virus lymphadenitis can mimic angioimmunoblastic T-cell lymphoma morphologically, immunophenotypically, and genetically: a case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5496818&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100147X%2Fabstract%3Frss%3Dyes</link>
            <description>We report the case of a young man who developed progressive diffuse lymphadenopathy with associated extremely high levels of serum Epstein-Barr virus in the setting of chronic immunosuppressive treatment of glomerulonephritis. Excisional biopsy of a right inguinal node revealed a sclerosing process with the morphologic appearance of angioimmunoblastic T-cell lymphoma with a CD3+, CD4+ immunophenotype. In situ hybridization of Epstein-Barr virus–encoded RNA was positive. Molecular probe studies demonstrated a clonal T-cell population. Upon reduction of immunosuppression, the patient's lymphadenopathy and Epstein-Barr virus titer have resolved without recurrence over 2 years time. This case demonstrates that a benign Epstein-Barr virus–associated process can mimic angioimmunoblastic T-ce...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496818</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496818</guid>        </item>
        <item>
            <title>Complex analysis of a recurrent pleomorphic hyalinizing angiectatic tumor of soft parts</title>
            <link>http://www.medworm.com/index.php?rid=5496817&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001432%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Pleomorphic hyalinizing angiectatic tumor of soft parts is a recently recognized, low-grade mesenchymal neoplasm of uncertain lineage. It is characterized by clusters of ectatic, fibrin-lined, thin-walled vessels surrounded by pleomorphic but mitotically inert spindled cells with frequent intranuclear inclusions and a variable inflammatory component. Here, we report a case of recurrent pleomorphic hyalinizing angiectatic tumor in a 37-year-old white woman. Touch imprint cytologic analysis revealed oval and spindled cells with fine chromatin, occasional prominent intranuclear inclusions, and intracytoplasmic pigment. The histologic features of the cells constituting the bulk of tumor were those characteristic of a putative precursor lesion (“early pleomorphic hyalinizing angiecta...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496817</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496817</guid>        </item>
        <item>
            <title>Acquired glomerular lesions in patients with Down syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5496812&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001638%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: The long-term survival of persons with Down syndrome has dramatically increased over the past 50 years. There are no studies addressing the spectrum of glomerular lesions in these patients. We reviewed the clinical-pathologic characteristics of 17 patients with Down syndrome who underwent renal biopsy. The cohort consisted of 12 whites and 5 African Americans with mean age of 29 years (range, 6-45 years). History of hypothyroidism was present in 8 patients. Renal presentations included renal insufficiency (15 patients, mean serum creatinine 3.4 mg/dL), proteinuria (all patients, including 3 with nephrotic syndrome, mean 24-hour urine protein 4.2 g), and hematuria (14 patients, including 4 with gross hematuria). The glomerular diseases found on biopsy were IgA nephropathy (n = 5 pa...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496812</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496812</guid>        </item>
        <item>
            <title>The hormone receptor, human epidermal growth factor receptor 2, and molecular subtype status of individual tumor foci in multifocal/multicentric invasive ductal carcinoma of breast</title>
            <link>http://www.medworm.com/index.php?rid=5496808&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001560%2Fabstract%3Frss%3Dyes</link>
            <description>This study was designed to evaluate the status of the hormone receptors, human epidermal growth factor receptor 2, and its molecular subtypes in individual foci of multifocal/multicentric invasive ductal carcinoma of the breast and to identify the factors associated with the different phenotypes of individual foci. We performed immunohistochemical analyses of the estrogen receptor, progesterone receptor, cytokeratin 5/6, epidermal growth factor receptor, and p53 and fluorescence in situ hybridization of human epidermal growth factor receptor 2 in individual foci of 65 cases of multifocal/multicentric invasive ductal carcinoma and the associated ductal carcinoma in situ components using tissue microarrays. The estrogen receptor status differed in 2 (3%) of the 65 invasive ductal carcinomas,...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496808</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496808</guid>        </item>
        <item>
            <title>Frameshift mutations of vacuolar protein sorting genes in gastric and colorectal cancers with microsatellite instability</title>
            <link>http://www.medworm.com/index.php?rid=5496807&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001559%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Vacuolar protein sorting plays crucial roles in the traffic of molecules between cellular organelles. Although involvement of vacuolar protein sorting proteins in cancer is known, genetic alterations of VPS genes have not been reported in cancers. We found that VPS4B, VPS13A, VPS13B, VPS13C, VPS33A, VPS35, VPS37B, VPS37D, VPS41, and VPS54 have mononucleotide repeats in their coding sequences. To see whether these genes are mutated in cancers with microsatellite instability, we analyzed the mononucleotide repeats in 30 gastric cancers with high microsatellite instability, 13 gastric cancers with low microsatellite instability, and 45 gastric cancers with stable microsatellites and 40 colorectal cancers with high microsatellite instability, 14 colorectal cancers with low microsatell...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5496807</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5496807</guid>        </item>
        <item>
            <title>Interobserver agreement for Polyomavirus nephropathy grading in renal allografts using the working proposal from the 10th Banff Conference on Allograft Pathology</title>
            <link>http://www.medworm.com/index.php?rid=5402044&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001535%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: A classification schema for grading Polyomavirus nephropathy was proposed at the 2009 Banff allograft meeting. The schema included 3 stages of Polyomavirus nephropathy: early (stage A), florid (stage B), and late sclerosing (stage C). Grading categories for histologic viral load levels were also proposed. To examine the applicability and the interobserver agreement of the proposed Polyomavirus nephropathy grading schema, we evaluated 24 renal allograft biopsies with confirmed Polyomavirus nephropathy by histology and SV40. Four renal pathologists independently scored the Polyomavirus nephropathy stage (A, B, or C), without knowledge of the clinical history. Viral load was scored as a percent of tubules exhibiting viral replication, using either a 3-tier viral load score (1: ≤1%;...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402044</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402044</guid>        </item>
        <item>
            <title>Senescence in intraductal papillary mucinous neoplasm of the pancreas</title>
            <link>http://www.medworm.com/index.php?rid=5402043&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001523%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Intraductal papillary mucinous neoplasm of the pancreas is attracting attention as a precursor lesion of the invasive ductal adenocarcinoma, whereas it has been reported that some intraductal papillary mucinous neoplasms do not display progression to malignancy and remain almost unchanged in size and morphology. Recent studies have reported that oncogene-induced senescence has been observed in neoplasms, especially in premalignant lesions, and that it can play an important role in preventing malignant progression. To clarify the presence of senescence in intraductal papillary mucinous neoplasms, we analyzed the expression of several markers of senescence. The intraductal papillary mucinous neoplasms evaluated in this study were classified into 4 groups according to the degree of d...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402043</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402043</guid>        </item>
        <item>
            <title>Cross-talk between chronic lymphocytic leukemia cells and bone marrow endothelial cells: role of signal transducer and activator of transcription 3</title>
            <link>http://www.medworm.com/index.php?rid=5402041&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100150X%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Chronic lymphocytic leukemia bone marrow is characterized by increased angiogenesis. However, the molecular mediators of neovascularization and the biologic significance of increased endothelial cell proliferation in chronic lymphocytic leukemia require further investigation. Because signal transducer and activator of transcription 3 is constitutively activated in chronic lymphocytic leukemia, we studied the role of signal transducer and activator of transcription 3 in modulating vascular endothelial growth factor expression and the effect of vascular endothelial cells on chronic lymphocytic leukemia cells. Using chromatin immunoprecipitation, we found that anti–signal transducer and activator of transcription 3 antibodies immunoprecipitated DNA of signal transducer and activato...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402041</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402041</guid>        </item>
        <item>
            <title>Renal medullary carcinomas: histopathologic phenotype associated with diverse genotypes</title>
            <link>http://www.medworm.com/index.php?rid=5402040&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001493%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Chromosomal abnormalities and gene mutations have become major determinants in the classification of kidney carcinomas. Most renal medullary carcinomas develop in patients with hereditary sickle cell disease, but sporadic cases unassociated with sickle cell disease have also been described, for which underlying genetic abnormality is unknown. We evaluated 3 patients with renal medullary carcinoma (1 patient with sickle cell disease and 2 patients without sickle cell disease) for germ line and somatic mutations in genes commonly involved in pathogenesis of renal carcinomas using denaturing high-performance liquid chromatography and direct sequencing. Chromosomal abnormalities were studied by the conventional cytogenetic and SNP arrays analysis. Expression of hypoxia-inducible facto...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402040</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402040</guid>        </item>
        <item>
            <title>Hyperplastic polyp of the duodenum: a report of 9 cases with immunohistochemical and molecular findings</title>
            <link>http://www.medworm.com/index.php?rid=5402037&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001195%2Fabstract%3Frss%3Dyes</link>
            <description>We report a series of 9 serrated polyps arising in the duodenum with clinicopathologic features, immunohistochemical expression profile of mucins (MUC2, MUC5AC, MUC6), and molecular analysis for BRAF and KRAS. The polyps were diagnosed as incidental endoscopy findings in 9 different patients, comprising 3 male and 6 female patients, with a mean age of 52.2 years (range, 21-72 years). The second part of the duodenum was the most common site (n = 5), followed by the ampulla (n = 1) and the distal duodenum (n = 1), with the location of the 2 remaining polyps unspecified. Other upper gastrointestinal tract pathology features included Barrett esophagus for 5 patients, Helicobacter gastritis for 1 patient, and mild chronic gastritis for 1 patient. The histologic appearance of the polyps was simi...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402037</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402037</guid>        </item>
        <item>
            <title>Small cell carcinoma of the kidney: a clinicopathologic study of 14 cases</title>
            <link>http://www.medworm.com/index.php?rid=5366955&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001456%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Small cell carcinoma of the kidney is distinctively rare. We searched pathology files in 2 institutions and found 14 cases of renal small cell carcinoma. The patients' mean age at diagnosis was 59 years (range, 22-75 years); 8 were women, and 6 were men. Patients usually presented with hematuria (n = 6) and abdominal pain (n = 5). The mean tumor size was 7.1 cm (range, 3.5-14.0 cm). The small cell carcinoma was pure in 9 cases and mixed with high-grade urothelial carcinoma in 5 cases. None was associated with any type of renal cell carcinoma. Tumor necrosis was present in all cases, and lymphovascular invasion was identified in 6 cases. The tumor invaded the perinephric adipose tissue in 13 cases and was confined to the kidney in only 1 case. Lymph node metastases were identified ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5366955</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5366955</guid>        </item>
        <item>
            <title>High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly</title>
            <link>http://www.medworm.com/index.php?rid=5366954&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001444%2Fabstract%3Frss%3Dyes</link>
            <description>In this study, we measured the frequency of unrecognized wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome. One hundred twenty-three patients with carpal tunnel syndrome, including 100 idiopathic patients, treated by carpal tunnel release surgery were analyzed. Tenosynovial tissues obtained at surgery were analyzed by Congo red and immunohistochemical staining. If staining for transthyretin was positive, the entire transthyretin gene was analyzed by direct DNA sequencing. We also analyzed tenosynovial tissues from 32 autopsy cases as controls. Thirty-four patients (34.0%) with idiopathic carpal tunnel syndrome showed amyloid deposition in the tenosynovial tissue, and all amyloid showed specific immunolabeling with antitransthyretin antibody. Direct DNA s...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5366954</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5366954</guid>        </item>
        <item>
            <title>Hepatocyte nuclear factor 4A expression discriminates gastric involvement by metastatic breast carcinomas from primary gastric adenocarcinomas</title>
            <link>http://www.medworm.com/index.php?rid=5366953&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001420%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Breast carcinomas sometimes metastasize to the stomach, and the histopathologic distinction of such metastases from primary gastric adenocarcinomas is often difficult. We characterized the clinicopathologic features of 21 breast carcinomas that had metastasized to the stomach and examined the use of a panel of antibodies, including hepatocyte nuclear factor 4A, for distinguishing the metastases from primary gastric diffuse-type adenocarcinomas. Histologically, all the metastatic breast carcinomas showed a poorly differentiated and/or signet ring cell morphology. Although most metastatic breast and primary gastric carcinomas contained signet ring cell components, the cases that were predominantly or exclusively composed of univacuolated-type signet ring cells were limited to metast...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5366953</comments>
            <pubDate>Wed, 06 Jul 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5366953</guid>        </item>
        <item>
            <title>S100P, von Hippel-Lindau gene product, and IMP3 serve as a useful immunohistochemical panel in the diagnosis of adenocarcinoma on endoscopic bile duct biopsy</title>
            <link>http://www.medworm.com/index.php?rid=5121512&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100222X%2Fabstract%3Frss%3Dyes</link>
            <description>We read with great interest the article by Levy et al concerning the value of S100P, von Hippel-Lindau gene product, and IMP3 as immunohistochemical markers in the biopsy diagnosis of bile duct carcinomas . Because biopsies from the biliary tract often show marked inflammation and reactive changes, the diagnosis of dysplasia/neoplasia is often very difficult or even impossible on pure morphologic grounds. Therefore, additional immunohistochemical markers helping in this differential diagnosis are clearly warranted. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5121512</comments>
            <pubDate>Sun, 26 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5121512</guid>        </item>
        <item>
            <title>Multiple chromosomal monosomies are characteristic of giant cell ependymoma</title>
            <link>http://www.medworm.com/index.php?rid=5402048&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001109%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Giant cell ependymoma, a rare ependymoma subtype, was recently recognized as a separate diagnostic entity with variations both in malignant potential and course of disease. We analyzed the first supratentorial giant cell ependymoma using G-band karyotyping, DNA ploidy analysis, and array comparative genomic hybridization. The tumor was hypodiploid, and the karyotype showed multiple monosomies. This novel cytogenetic pattern seems specific for giant cell ependymoma as the only previous cytogenetic analysis of a giant cell ependymoma found similar monosomies. We were also able to analyze cytogenetically the subsequent recurrent tumor, phenotypically an anaplastic ependymoma, allowing a first insight into the genetic events involved in disease progression. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402048</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402048</guid>        </item>
        <item>
            <title>Epstein-Barr virus–positive T-cell lymphoma cells having chromosome 22q11.2 deletion: an autopsy report of DiGeorge syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5402047&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001079%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Reported herein was the first autopsy case of Epstein-Barr virus–associated T-cell lymphoma in a 25-year-old man with DiGeorge syndrome. Systemic lymph nodes demonstrated diffuse encasement by large lymphoma cells positive for CD45, CD2, CD3, CD5, CD7, CD8, TIA1, and granzyme B, accompanied with marked hemophagocytosis. Almost 100% of lymphoma cells were both EBER- and LMP-1-positive, and EBNA2-negative. The rearrangement of T-cell receptor β gene was proved by polymerase chain reaction. Clinical and pathologic features coincided with Epstein-Barr virus–associated T/NK-cell lymphoproliferative disorder preceded by chronic active Epstein-Barr virus infection. A fluorescence in situ hybridization using paraffin-embedded tissues demonstrated a mosaic chromosome 22q11.2 deletion ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402047</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402047</guid>        </item>
        <item>
            <title>Hepatosplenic T-cell lymphoma: clinicopathologic, immunophenotypic, and molecular characterization of17 Chinese cases</title>
            <link>http://www.medworm.com/index.php?rid=5402039&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001213%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Hepatosplenic T-cell lymphoma is a highly aggressive tumor with a poor outcome. About 210 cases were identified through PubMed, of which fewer than 20 originated in Asia. We reviewed 17 Chinese cases of hepatosplenic T-cell lymphoma, including an unusual one with cutaneous pink papules, for clinicopathologic, immunophenotypic, and genotypic features; Epstein-Barr virus status; treatment; and outcome. The median age of the patients was 23 years. All patients had splenomegaly, and 88.2% of them had hepatomegaly as well. Bone marrow involvement was present in 53.3%. Eleven patients underwent splenectomy for diagnosis and treatment. Twelve specimens were collected by image-guided liver core biopsy or wedge resection. Histologically, the homogeneous small- to medium-size neoplastic lym...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402039</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402039</guid>        </item>
        <item>
            <title>Low activated leukocyte cell adhesion molecule expression is associated with advanced tumor stage and early prostate-specific antigen relapse in prostate cancer</title>
            <link>http://www.medworm.com/index.php?rid=5402036&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001158%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Activated leukocyte cell adhesion molecule (CD166) is a member of the immunoglobulin superfamily and is aberrantly expressed in different tumors, including prostate cancer. To learn more on the prevalence and clinical significance of activated leukocyte cell adhesion molecule expression in prostate cancer, a tissue microarray containing 3261 primary prostate cancers treated by radical prostatectomy was used. A total of 2390 different prostate cancers were analyzed by immunohistochemistry in a tissue microarray format. Activated leukocyte cell adhesion molecule immunostaining in cancers was compared with clinical follow-up, which was available for 1746 patients. Membranous activated leukocyte cell adhesion molecule immunostaining was recorded in 1663 (69.6%) of cases. High activate...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402036</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402036</guid>        </item>
        <item>
            <title>Centrosome amplification as a putative prognostic biomarker for the classification of urothelial carcinomas</title>
            <link>http://www.medworm.com/index.php?rid=5402033&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001110%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Recent studies have reported that centrosome amplification is closely related to chromosomal instability and patient prognosis in human malignancies. The purpose of this study was to elucidate the relationship between centrosome amplification and genomic alterations in urothelial carcinomas. Centrosomes were evaluated by immunohistochemistry using anti–γ-tubulin antibody. Array-based comparative genomic hybridization technology using DNA chips spotted with 4030 bacterial artificial chromosome clones was applied to 70 urothelial carcinomas to examine DNA copy number aberrations. Studying aberrations in the number of chromosomes 7, 9, and 17 using fluorescence in situ hybridization allowed the estimation of the degree of chromosomal instability. DNA copy number gains at 20p12.2, ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402033</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402033</guid>        </item>
        <item>
            <title>Illumina whole-genome complementary DNA–mediated annealing, selection, extension and ligation platform: assessing its performance in formalin-fixed, paraffin-embedded samples and identifying invasion pattern–related genes in oral squamous cell carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5402032&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001092%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: High-throughput gene expression profiling from formalin-fixed, paraffin-embedded tissues has become a reality, and several methods are now commercially available. The Illumina whole-genome complementary DNA–mediated annealing, selection, extension and ligation assay (Illumina, Inc) is a full-transcriptome version of the original 512-gene complementary DNA–mediated annealing, selection, extension and ligation assay, allowing high-throughput profiling of 24 526 annotated genes from degraded and formalin-fixed, paraffin-embedded RNA. This assay has the potential to allow identification of novel gene signatures associated with clinical outcome using banked archival pathology specimen resources. We tested the reproducibility of the whole-genome complementary DNA–mediated anneal...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402032</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402032</guid>        </item>
        <item>
            <title>Regenerating I messenger RNA and protein expression in the failing human testis: a potential molecular prognostic marker of seminoma</title>
            <link>http://www.medworm.com/index.php?rid=5402024&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001183%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Infertility has been stated as a risk factor for testicular cancer; but currently, there is no prognostic indicator of tumor development from the pathologic testis with impaired spermatogenesis. Regenerating proteins are expressed in many human tissues including the testis, and their role in carcinogenesis has been well documented. In the present work, regenerating I messenger RNA and protein expression and cellular protein localization were studied in testicular biopsies of patients with normal (obstructive azoospermia) or impaired spermatogenesis (nonobstructive azoospermia) and in seminoma testis by quantitative reverse transcriptase–polymerase chain reaction, Western blot, and immunofluorescence analyses. No significant differences in regenerating I transcripts were reported...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402024</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402024</guid>        </item>
        <item>
            <title>Prognostic significance of mitotic figures in metastatic mammary ductal carcinoma to the lymph nodes</title>
            <link>http://www.medworm.com/index.php?rid=5402022&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001134%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, this study clearly confirmed the excellent outcome predictive power of the number of mitotic figures in metastatic mammary carcinoma to the lymph nodes. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402022</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402022</guid>        </item>
        <item>
            <title>Limited smoothelin expression within the muscularis mucosae: validation in bladder diverticula</title>
            <link>http://www.medworm.com/index.php?rid=5366952&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001249%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Smoothelin, a marker of differentiated smooth muscle, is diffusely expressed by bladder muscularis propria and is negative to only weakly and focally expressed in muscularis mucosae. We used bladder diverticula, which lack muscularis propria and frequently demonstrate hyperplastic muscularis mucosae, to evaluate the use of smoothelin immunoreactivity in diagnostic pathology. Diverticula from 40 patients (21 with benign features, 19 with neoplastic features) were studied. Immunohistochemistry was performed using smoothelin antibody (clone R4A, 1:150 dilution; Abcam, Cambridge, MA); and tissue was scored as 0 (no expression), 1+ (moderate expression 10% of cells), and 3+ (robust diffuse expression). All diverticula contained muscularis mucosae of varying caliber; staining in diverti...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5366952</comments>
            <pubDate>Mon, 20 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5366952</guid>        </item>
        <item>
            <title>Erratum to “Overexpression of Cullin 1 is associated with poor prognosis of patients with gastric cancer” [Hum Pathol 2011; 42:375-383]</title>
            <link>http://www.medworm.com/index.php?rid=4940473&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001419%2Fabstract%3Frss%3Dyes</link>
            <description>In the aforementioned article, the authors have noted an error in and regarding TNM stage. The correct numbers should read as follows: (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940473</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:22 +0100</pubDate>
            <guid isPermaLink="false">4940473</guid>        </item>
        <item>
            <title>Do mast cell phenotypes play a role in concomitantly increased microvessel density and progression of non–small cell lung cancer?—reply</title>
            <link>http://www.medworm.com/index.php?rid=4940472&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000980%2Fabstract%3Frss%3Dyes</link>
            <description>Mast cells are multifaceted immune cells that participate in both physiologic and pathologic settings. In cancer, whether mast cells promote or inhibit tumor growth has stimulated much discussion but remains an unanswered question. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940472</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:22 +0100</pubDate>
            <guid isPermaLink="false">4940472</guid>        </item>
        <item>
            <title>Do mast cell phenotypes play a role in concomitantly increased microvessel density and progression of non–small cell lung cancer?</title>
            <link>http://www.medworm.com/index.php?rid=4940471&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000967%2Fabstract%3Frss%3Dyes</link>
            <description>I read the article by Carlini et al describing “Mast cell phenotypes and microvessels in non–small cell lung cancer and its prognostic significance” with great interest. Our concern in this article is that we recently demonstrated in vitro human mast cell (MC)–mediated cytotoxicity against different human tumor cells . Although the authors mentioned MCs' probable tumor-inhibitory role, their dominant opinion in this topic is the tumor-promoting role of MCs. Thus, this article may cause a false impression about MCs as being associated with tumor progression in non–small cell lung cancer (NSCLC). In contrast to their findings, many articles have found an association between increased mast cell density (MCD) and good prognosis in different tumors, including NSCLC. (Source: Human Pat...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940471</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:21 +0100</pubDate>
            <guid isPermaLink="false">4940471</guid>        </item>
        <item>
            <title>Thyroid transcription factor 1 expression in endometrioid tumors: a note of caution—reply</title>
            <link>http://www.medworm.com/index.php?rid=4940470&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100092X%2Fabstract%3Frss%3Dyes</link>
            <description>We greatly appreciate the comments by Cameselle-Teijeiro et al. We agree with them in that positive reactions in morula cells, which have a high content of endogenous biotin, are a potential pitfall in immunohistochemical analysis of a variety of tissues. Endogenous biotin is rich in hepatocytes, kidneys, and adrenal cortex, whereas biotin-like activity has been also documented . In addition, biotin can be located in nuclei in specific instances, most of which have been reported in association with morula in various organs. Histologically, such cells can be recognized as those showed optically clear nuclei, which ultrastructurally constitute filamentous structures . These cells show nonspecific positive immunohistochemical reactions because of binding to endogenous biotin, and such reactio...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940470</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:21 +0100</pubDate>
            <guid isPermaLink="false">4940470</guid>        </item>
        <item>
            <title>Thyroid transcription factor-1 expression in endometrioid tumors: a note of caution</title>
            <link>http://www.medworm.com/index.php?rid=4940469&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000931%2Fabstract%3Frss%3Dyes</link>
            <description>With great interest, we read the article by Fujiwara et al published in the April 2010 issue of Human Pathology. These authors concluded that thyroid transcription factor 1 (TTF1) is expressed in gynecologic malignancies and that this expression confers a better prognosis in patients with ovarian cancer. However, because of the fact that the study was made using an avidin-biotin immunoperoxidase technique after heat-induced epitope retrieval and because of the nature of specimens, we find some comments necessary for the appropriate interpretation of these findings. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940469</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:21 +0100</pubDate>
            <guid isPermaLink="false">4940469</guid>        </item>
        <item>
            <title>Molecular pathogenesis and extraovarian origin of epithelial ovarian cancer—Shifting the paradigm</title>
            <link>http://www.medworm.com/index.php?rid=4940452&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001377%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Recent morphologic, immunohistochemical, and molecular genetic studies have led to the development of a new paradigm for the pathogenesis and origin of epithelial ovarian cancer based on a dualistic model of carcinogenesis that divides epithelial ovarian cancer into 2 broad categories designated types I and II. Type I tumors comprise low-grade serous, low-grade endometrioid, clear cell and mucinous carcinomas, and Brenner tumors. They are generally indolent, present in stage I (tumor confined to the ovary), and are characterized by specific mutations, including KRAS, BRAF, ERBB2, CTNNB1, PTEN, PIK3CA, ARID1A, and PPP2R1A, which target specific cell signaling pathways. Type I tumors rarely harbor TP53 mutations and are relatively stable genetically. Type II tumors comprise high-gra...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940452</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:13 +0100</pubDate>
            <guid isPermaLink="false">4940452</guid>        </item>
        <item>
            <title>On Being a Pathologist: Maria Dąbska - the woman behind the eponym, a pioneer in pathology</title>
            <link>http://www.medworm.com/index.php?rid=4940451&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001602%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: There is only one cancer to our knowledge named in honor of its female describer, the Dąbska tumor. Maria Dąbska was a brave hero of the Warsaw Resurrection of 1944 who survived deportation to Germany to graduate from medical school in Gdańsk and pursue a career in pathology, for which her research on the Dąbska tumor, breast cancer, sweat gland tumors, keratoacanthoma, soft tissue sarcomas, bone pathology, parachordoma, melanoma, and other entities remains salient. Working behind the Iron Curtain, she nevertheless achieved international recognition, yet few today are cognizant of her and her accomplishments. This vibrant distinguished professor is celebrating her 90th birthday. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940451</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:12 +0100</pubDate>
            <guid isPermaLink="false">4940451</guid>        </item>
        <item>
            <title>In This Issue</title>
            <link>http://www.medworm.com/index.php?rid=4940450&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002280%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940450</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:12 +0100</pubDate>
            <guid isPermaLink="false">4940450</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=4940449&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002279%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940449</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:12 +0100</pubDate>
            <guid isPermaLink="false">4940449</guid>        </item>
        <item>
            <title>Table of Contents</title>
            <link>http://www.medworm.com/index.php?rid=4940448&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002267%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940448</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:12 +0100</pubDate>
            <guid isPermaLink="false">4940448</guid>        </item>
        <item>
            <title>Editorial Board</title>
            <link>http://www.medworm.com/index.php?rid=4940447&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002255%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940447</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:12 +0100</pubDate>
            <guid isPermaLink="false">4940447</guid>        </item>
        <item>
            <title>Masthead</title>
            <link>http://www.medworm.com/index.php?rid=4940446&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711002243%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4940446</comments>
            <pubDate>Sat, 18 Jun 2011 23:17:12 +0100</pubDate>
            <guid isPermaLink="false">4940446</guid>        </item>
        <item>
            <title>Oncocytic mucoepidermoid carcinoma of the parotid gland with CRTC1-MAML2 fusion transcript: report of a case with review of literature</title>
            <link>http://www.medworm.com/index.php?rid=5402050&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001237%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Oncocytic mucoepidermoid carcinoma is a very rare variant of mucoepidermoid carcinoma, composed predominantly of oncocytic cells. Most previously reported cases described the difficulty in histologic differentiation from other oncocytic tumors. Here we report a case of oncocytic mucoepidermoid carcinoma of parotid gland diagnosed by the detection of CRTC1-MAML2 fusion. A 53-year-old man had a left superficial parotidectomy conducted for 3-cm-sized mass. The resected tumor was composed almost exclusively of oncocytic tumor cells. With detailed histologic evaluation, scarce vacuolated tumor cells, suggestive of mucous cell of mucoepidermoid carcinoma, and one focus of tumor embolism in a vein were found, suggesting the possibility of oncocytic mucoepidermoid carcinoma. Immunohistoch...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402050</comments>
            <pubDate>Wed, 15 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402050</guid>        </item>
        <item>
            <title>Medulloepithelioma of the optic disc</title>
            <link>http://www.medworm.com/index.php?rid=5402049&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001225%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: A 6-year-old boy with a history of an amblyopic, occasionally red left eye was found to have a solid white mass overlying the optic disc on dilated ocular fundus examination. Transvitreal endoincisional biopsy of the mass yielded neoplastic tissue consistent with intraocular medulloepithelioma. The eye was removed subsequently because of concern that the tumor may invade the retrobulbar optic nerve. Histopathologic and immunohistochemical analysis of the tumor confirmed nonteratoid medulloepithelioma of the optic disc. The child has been followed up for over 36 months without any signs of orbital tumor recurrence or metastasis. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402049</comments>
            <pubDate>Wed, 15 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402049</guid>        </item>
        <item>
            <title>t(4;22)(q12;q11.2) involving presumptive platelet-derived growth factor receptor A and break cluster region in a patient with mixed phenotype acute leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5402046&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001067%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: The patient is a 45-year-old woman with a history of breast cancer who had been treated 1 year ago with radiation and chemotherapy. Flow cytometric analysis of bone marrow aspirate revealed 81% blasts positive for CD4, CD11c (partial), CD13, CD19 (partial), cytoplasmic CD22, CD34, CD36, CD45, cytoplasmic CD79a, CD117 (partial), HLA-DR, and terminal deoxynucleotide transferase, consistent with a mixed phenotype acute leukemia (B/myeloid lineage). Conventional karyotypic analysis revealed a t(4;22)(q12;q11.2) in 12 of 13 cells analyzed. Fluorescence in situ hybridization analysis using a dual-color, dual-fusion break cluster region/ABL probe set showed no break cluster region/ABL translocation but an extra break cluster region signal in 85% (170/200) of cells, consistent with a tran...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402046</comments>
            <pubDate>Wed, 15 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402046</guid>        </item>
        <item>
            <title>Association between natural killer cells and regression in melanocytic lesions</title>
            <link>http://www.medworm.com/index.php?rid=5402038&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001201%2Fabstract%3Frss%3Dyes</link>
            <description>In this study, the goal was to determine if natural killer cells are preferentially involved in the cytotoxic response in regressing lesions. Forty-two cases were selected: nevi with regression, nonregressing melanoma with brisk inflammation, and regressing melanoma. Sections were stained with hematoxylin and eosin and immunostained for CD8, CD56, and T-cell intracytoplasmic antigen 1. Numbers of total lymphocytes, CD8-positive lymphocytes, and T-cell intracytoplasmic antigen 1–positive lymphocytes did not differ among the 3 populations or based on location. CD56 positivity was significantly different among the 3 populations. Regressing melanomas showed the greatest CD56 activity, followed by regressing nevi, whereas inflamed, nonregressing melanomas showed the least. CD56+ lymphocytes w...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402038</comments>
            <pubDate>Wed, 15 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402038</guid>        </item>
        <item>
            <title>Correlation between genomic alterations assessed by array comparative genomic hybridization, prognostically informative histologic subtype, stage, and patient survival in gastric cancer</title>
            <link>http://www.medworm.com/index.php?rid=5402035&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001146%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: It is difficult to evaluate the prognostic value of histologic criteria in gastric cancer because of the high variability of morphologic patterns. Recently, histologic subtypes of low, intermediate, or high malignant potential have been identified, providing the basis for a prognostically informative grading system. Because array comparative genomic hybridization systems allow systematic analysis of chromosome alterations, which may be prognostically and pathogenetically informative, we applied high-resolution genome-wide array comparative genomic hybridization to archival material from 81 gastric cancer cases followed for a median of 150 months after surgery. The DNA extracted from paraffin sections gave useful results in 49 tumors, 18 of which were of low-grade, 24 of intermedia...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402035</comments>
            <pubDate>Wed, 15 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402035</guid>        </item>
        <item>
            <title>Immunohistochemical expression of prostate tumor overexpressed 1 in cystoprostatectomies with incidental and insignificant prostate cancer. Further evidence for field effect in prostatic carcinogenesis</title>
            <link>http://www.medworm.com/index.php?rid=5402034&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001122%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, our findings related to prostate tumor overexpressed 1 expression in high-grade prostatic intraepithelial neoplasia, evaluated adjacent and away from prostate cancer, and in incidental and clinical cancers give further support to the concept of field effect in prostatic carcinogenesis as well as to differences in the process of prostatic carcinogenesis between cystoprostatectomies and radical prostatectomies. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402034</comments>
            <pubDate>Wed, 15 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402034</guid>        </item>
        <item>
            <title>Genetic alterations and protein expression of HER2 and chromosome 17 polysomy in breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5263412&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001080%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: HER2/neu alteration detection in breast cancer is important for decision making of the HER2-targeted therapy. We retrospectively analyzed the HER2/neu status by fluorescence in situ hybridization and HER2 protein expression by immunohistochemistry in a cohort of 481 patients with invasive breast cancer. Fluorescence in situ hybridization showed that 57.4% of cases exhibited HER2 amplification but 41.4% did not, and 1.2% exhibited an equivocal status. Immunohistochemistry showed that 10.4%, 16.8%, 38.3%, and 34.5% of cases had scores of 0, 1+, 2+, and 3+, respectively. The HER2 status showed a moderate agreement with HER2 expression with a score of 0, 1+, and 3+ (κ = 0.576, P &lt; .05), and the concordance rate was 90%, 61.7%, and 83.1%, respectively. The HER2 amplification occurred ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5263412</comments>
            <pubDate>Wed, 15 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5263412</guid>        </item>
        <item>
            <title>Distinctive patterns of p53 protein expression and microsatellite instability in human colorectal cancer</title>
            <link>http://www.medworm.com/index.php?rid=5402031&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001055%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, a restricted pattern of p53 overexpression is preferentially associated with microsatellite instability high phenotype and could, therefore, be of clinical use as signal for microsatellite instability analysis in a large-scale tumor screening. Its association with concomitant murine double minute 2 overexpression suggests an alternative mechanism of p53 pathway deregulation. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402031</comments>
            <pubDate>Mon, 13 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402031</guid>        </item>
        <item>
            <title>Systematic analysis of proteins from different signaling pathways in the tumor center and the invasive front of colorectal cancer</title>
            <link>http://www.medworm.com/index.php?rid=5402030&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001043%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: In colorectal cancer, the functional impact of proteins from different signaling pathways varies between tumor center and tumor front. Our objective was to identify differential protein expression profiles between the tumor center and the tumor front of colorectal cancer. Twenty proteins from different signaling pathways (epidermal growth factor receptor [EGFR], phosphorylated extracellular signal regulated kinase [pERK], receptor for hyalouronic acid mediated motility [RHAMM], Raf-1 kinase inhibitor protein [RKIP], β-catenin, E-cadherin, phosphorylated AK transforming [pAKT], p16, p21, Ki-67, B-cell Lymphoma-2 [BCL2], vascular endothelial growth factor, apoptosis protease activating factor 1 [APAF-1], mucin1 [MUC1], ephrin B2 receptor [EphB2], matrix metalloproteinase 7 [MMP7], ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402030</comments>
            <pubDate>Mon, 13 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402030</guid>        </item>
        <item>
            <title>Intratumoral budding as a potential parameter of tumor progression in mismatch repair–proficient and mismatch repair–deficient colorectal cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5402023&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100102X%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: In colorectal cancer, tumor budding at the invasive front (peritumoral budding) is an established prognostic parameter and decreased in mismatch repair–deficient tumors. In contrast, the clinical relevance of tumor budding within the tumor center (intratumoral budding) is not yet known. The aim of the study was to determine the correlation of intratumoral budding with peritumoral budding and mismatch repair status and the prognostic impact of intratumoral budding using 2 independent patient cohorts. Following pancytokeratin staining of whole-tissue sections and multiple-punch tissue microarrays, 2 independent cohorts (group 1: n = 289; group 2: n = 222) with known mismatch repair status were investigated for intratumoral budding and peritumoral budding. In group 1, intratumoral ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402023</comments>
            <pubDate>Mon, 13 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402023</guid>        </item>
        <item>
            <title>Intraglomerular crescentic metastases of malignant melanoma</title>
            <link>http://www.medworm.com/index.php?rid=5402045&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001031%2Fabstract%3Frss%3Dyes</link>
            <description>We describe here a patient with a metastatic malignant melanoma displaying crescentic lesions in the glomeruli. A 64-year-old woman was referred to our hospital because of a sudden increase of serum creatinine. Clinical diagnosis suggested rapidly progressive glomerulonephritis. Renal biopsy revealed diffuse crescentic lesions containing metastatic melanoma cells. These cells were also seen in the glomerular capillary lumina and tubules, and a few scattered tumor cells were also present in the interstitium. Glomerular metastasis is a very rare entity. To the best of our knowledge, this patient is the first to be described in the English language literature showing intraglomerular metastasis of malignant melanoma as demonstrated by needle biopsy and is only the second patient with intraglom...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402045</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402045</guid>        </item>
        <item>
            <title>Parakeratosis in skin is associated with loss of inhibitor of differentiation 4 via promoter methylation</title>
            <link>http://www.medworm.com/index.php?rid=5402029&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000918%2Fabstract%3Frss%3Dyes</link>
            <description>In this study, we addressed specificity by immunohistochemical staining for inhibitor of differentiation 4 protein in skin disorders showing parakeratosis, including: psoriasis (n = 9), chronic eczema (n = 6), and squamous cell carcinoma (n = 7). In these conditions, parakeratotic keratinocytes in the upper layers of the skin lacked inhibitor of differentiation 4 protein expression, whereas keratinocytes in the lower layers were densely stained, in contrast to diffuse expression in normal skin. Because promoter hypermethylation of inhibitor of differentiation 4 has been described in several cancers, we determined the methylation pattern of the inhibitor of differentiation 4 promoter in psoriasis and compared this with squamous cell carcinoma. We found a novel methylation pattern of the inh...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402029</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402029</guid>        </item>
        <item>
            <title>PAX8 immunostaining of anaplastic thyroid carcinoma: a reliable means of discerning thyroid origin for undifferentiated tumors of the head and neck</title>
            <link>http://www.medworm.com/index.php?rid=5402028&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS004681771100089X%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Anaplastic thyroid carcinoma can be difficult to diagnose because it does not show thyroid differentiation morphologically or immunohistochemically. Depending on the histologic variant, anaplastic thyroid carcinoma may be confused with sarcoma or squamous cell carcinoma of the head and neck. PAX8 is a transcription factor expressed in normal and neoplastic thyroid follicular epithelium and only a few other tissues. This restricted expression suggests that PAX8 staining could be useful when dealing with spindled or squamoid tumors of the neck. The purposes of this study were to determine the frequency of PAX8 staining in anaplastic thyroid carcinoma and to evaluate PAX8 immunohistochemistry as a means of distinguishing its squamoid variant from head and neck squamous cell carcinoma...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402028</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402028</guid>        </item>
        <item>
            <title>Expression of nitric oxide synthases in primary ciliary dyskinesia</title>
            <link>http://www.medworm.com/index.php?rid=5402026&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000876%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Nitric oxide is believed to play a central role in nonspecific defense of upper airways. Patients with primary ciliary dyskinesia have very low concentration of nasal nitric oxide, which may contribute to the chronic upper airway diseases encountered by these patients. The mechanisms underlying this drop of nasal nitric oxide in primary ciliary dyskinesia are still unknown. The goal of the present work was to study nitric oxide synthases expression in upper airway tissues from patients with primary ciliary dyskinesia. For this purpose, 5 patients with primary ciliary dyskinesia and 10 nonallergic age-matched patients without primary ciliary dyskinesia undergoing nasal polypectomy were included. Nasal nitric oxide concentration was measured before polypectomy, and nitric oxide synt...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402026</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402026</guid>        </item>
        <item>
            <title>Frequency, phenotype, and genotype of minute gastrointestinal stromal tumors in the stomach: an autopsy study</title>
            <link>http://www.medworm.com/index.php?rid=5402025&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000839%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Gastrointestinal stromal tumors are the most common mesenchymal tumors of the human digestive tract. Up to 85% of these tumors show somatic gain-of-function mutation of the receptor tyrosine kinase c-KIT gene. A recent study has shown a high frequency (22.5%) of minute gastrointestinal stromal tumors in stomachs examined during routine autopsies. The aims of our study were to confirm the previously reported incidence of gastric gastrointestinal stromal tumors in routine autopsies and to investigate their molecular alterations. Gastrointestinal stromal tumors were collected prospectively from 578 autopsies over an 18-month period. After recording the size and location of each lesion, representative tissue samples were processed for hematoxylin and eosin staining and immunohistochem...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402025</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402025</guid>        </item>
        <item>
            <title>Endobronchial metastatic breast cancer with pagetoid histology mimicking bronchial pagetoid squamous cell carcinoma in situ</title>
            <link>http://www.medworm.com/index.php?rid=5325926&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001018%2Fabstract%3Frss%3Dyes</link>
            <description>This report raises awareness of this uncommon manifestation of metastatic breast cancer. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325926</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325926</guid>        </item>
        <item>
            <title>Benign lymphoid hyperplasia (pseudolymphoma) of soft tissue</title>
            <link>http://www.medworm.com/index.php?rid=5325925&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000943%2Fabstract%3Frss%3Dyes</link>
            <description>We describe a case of a pseudolymphoma of the deep soft tissues of the lower extremity. The lesion was composed of nonencapsulated lymphoid tissue with involvement of adjacent fat and connective tissues and multiple variably sized well-polarized germinal centers. Immunohistochemical staining, flow cytometry, chromogenic in situ hybridization for κ/λ light-chain restriction, and polymerase chain reaction for T- and B-cell gene rearrangements all revealed a polyclonal population of T and B cells, consistent with a benign reactive process. So far as we know, pseudolymphoma of the deep soft tissues has been described only once previously in the medical literature. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325925</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325925</guid>        </item>
        <item>
            <title>Anaplastic lymphoma kinase–positive anaplastic large cell lymphoma presenting as retroperitoneal fibrosis</title>
            <link>http://www.medworm.com/index.php?rid=5325924&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000840%2Fabstract%3Frss%3Dyes</link>
            <description>We describe in this case report a highly unusual presentation of a young woman who died with a diagnosis of “idiopathic retroperitoneal fibrosis” based on multiple biopsy procedures. Postmortem examination, however, revealed disseminated anaplastic lymphoma kinase–positive anaplastic large cell lymphoma. The clinical and histopathologic importance of this very unusual presentation of anaplastic lymphoma kinase–positive anaplastic large cell lymphoma with retroperitoneal fibrosis is discussed. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325924</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325924</guid>        </item>
        <item>
            <title>Breast cancer multifocality, disease extent, and survival</title>
            <link>http://www.medworm.com/index.php?rid=5325922&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000864%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: The prognostic information implied in subgross morphologic parameters such as lesion distribution (unifocal, multifocal, or diffuse) and disease extent in breast cancer has remained largely unexplored in the literature. We aimed to test whether these parameters influence survival in breast carcinoma. The parameters were assessed in a series of 574 cases, all documented in large-format histology sections. We used Cox proportional hazards regression accompanied by Kaplan-Meyer survival curves, with P &lt; .05 regarded as significant. The invasive component was unifocal in 62% (311/499), multifocal in 24% (122/499), and diffuse in 5% (26/499) of the cases. Combining the in situ and invasive tumor components resulted in 48% (274/574) unifocal, 25% (141/574) multifocal, and 20% (117/574) ...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325922</comments>
            <pubDate>Fri, 10 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325922</guid>        </item>
        <item>
            <title>Benign mesothelial cells as confounders when cytokeratin immunohistochemistry is used in sentinel lymph nodes</title>
            <link>http://www.medworm.com/index.php?rid=5032305&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001006%2Fabstract%3Frss%3Dyes</link>
            <description>We read with interest the article by Dr Marchevsky et al assessing the presence and significance of isolated tumor cells and micrometastases in the intrathoracic lymph nodes of individuals undergoing surgery for non–small cell lung carcinoma (NSCLC). They examined 4188 lymph nodes from 266 consecutive clinical stage I NSCLC patients undergoing surgery. One hundred ninety-seven (74%) of these patients were pN0 by routine analysis. After examination with immunohistochemistry (IHC) for AE1/AE3, 7 patients were upstaged from pN0 to pN0(i+) (presence of single cells), 27 were upstaged from pN0 to pN1(mi) (presence of micrometastases), 3 from pN0 to pN2(mi), and 25 from pN1 to pN2(mi). However, this upstaging based on IHC did not predict difference in survival; and the authors conclude that ro...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032305</comments>
            <pubDate>Thu, 09 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5032305</guid>        </item>
        <item>
            <title>Critical regions and spreading of runt-related transcription factor-3 C-phosphate-G (CpG) island methylation in human salivary gland adenoid cystic carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5402027&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000888%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: We investigated the spreading pattern of runt-related transcription factor-3 (RUNX3) C-phosphate-G (CpG) island (3478 base pairs) methylation in salivary gland adenoid cystic carcinoma. The methylation status of multiple regions within the runt-related transcription factor-3 promoter CpG island (3478 base pairs) was detected by real-time methylation-specific polymerase chain reaction, and the runt-related transcription factor-3 protein was detected with a Western blot in 19 salivary gland adenoid cystic carcinoma samples and the corresponding nonneoplastic salivary glands. The risk ratio between runt-related transcription factor-3 CpG island methylation and salivary gland adenoid cystic carcinoma progression was analyzed by the logistic analysis of variance model. A possible assoc...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5402027</comments>
            <pubDate>Thu, 09 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5402027</guid>        </item>
        <item>
            <title>Low-grade fibromyxoid sarcoma of the perineum with heterotopic ossification: case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5325923&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000827%2Fabstract%3Frss%3Dyes</link>
            <description>We present a case of an ossifying tumor of the perineum that required an open biopsy and fluorescent in situ hybridization testing for FUS and CREB3L2 for diagnosis as a variant of low-grade fibromyxoid sarcoma. Subsequent excision revealed characteristic areas with collagen rosettes as well as foci of heterotopic ossification. Significant ossification, which is well documented in entities such as synovial sarcoma, ossifying fibromyxoid tumor, and extraskeletal osteosarcoma, has not been reported previously in low-grade fibromyxoid sarcoma. This case demonstrates the value of having a distinctive confirmatory molecular pathology test for diagnosis and expands our knowledge of the histologic variants possible in low-grade fibromyxoid sarcoma. (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325923</comments>
            <pubDate>Thu, 09 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325923</guid>        </item>
        <item>
            <title>Renal small cell oncocytoma with pseudorosettes: A histomorphologic, immunohistochemical, and molecular genetic study of 10 cases</title>
            <link>http://www.medworm.com/index.php?rid=5325921&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000815%2Fabstract%3Frss%3Dyes</link>
            <description>In conclusion, we herein present the first study on small cell renal oncocytomas with formation of pseudorosettes. This is a rare subtype of oncocytoma, which may, especially on a core biopsy, present differential diagnostic difficulties. The immunohistochemical profile of these tumors is variable and differs in significant respects from that of conventional renal oncocytoma. Awareness of this entity and its immunohistochemical variability should help in distinguishing this rare tumor from malignant tumors with similar (small cell) histomorphologic features. All tumors behaved in a benign fashion during follow-up (mean, 3.1 years; median, 1 year). (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325921</comments>
            <pubDate>Wed, 08 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325921</guid>        </item>
        <item>
            <title>α(1,6)Fucosyltransferase expression is an independent prognostic factor for disease-free survival in colorectal carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5325920&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000803%2Fabstract%3Frss%3Dyes</link>
            <description>Abstract: We previously reported that α(1,6)fucosyltransferase (Enzyme class 2.4.1.68) activity and expression are increased in colorectal cancer, suggesting a role for this enzyme in tumor development and progression. However, the possible impact of α(1,6)fucosyltransferase activity or expression on clinical outcomes in colorectal cancer patients has never been studied. Thus, the present study was conducted to determine the value of α(1,6)fucosyltransferase as a prognostic factor for colorectal cancer. α(1,6)Fucosyltransferase expression was analyzed using immunohistochemistry in 141 colorectal tumors, and α(1,6)fucosyltransferase activity was determined in 39 tumors. A complete standardized follow-up of patients was documented until the end of the observation period of 5 years or pa...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325920</comments>
            <pubDate>Wed, 08 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325920</guid>        </item>
        <item>
            <title>Activation of the phosphatidylinositol 3′-kinase/AKT pathway in neuroblastoma and its regulation by thioredoxin 1</title>
            <link>http://www.medworm.com/index.php?rid=5325919&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000657%2Fabstract%3Frss%3Dyes</link>
            <description>The objective of this study was to explore phosphatidylinositol 3′-kinase/AKT pathway activation and regulation by thioredoxin 1 to identify potential therapeutic targets. Immunohistochemical analysis was done on tissue microarrays from tumor samples of 101 patients, using antibodies against phosphatidylinositol 3′-kinase, AKT, activated AKT, phosphatase and tensin homolog, phosphorylated phosphatase and tensin homolog, thioredoxin 1, epidermal growth factor receptor, vascular endothelial growth factor and receptors (vascular endothelial growth factor 1 and vascular endothelial growth receptor 2), platelet-derived growth factor receptors, insulin-like growth factor 1 receptor, neurotrophic tyrosine kinase receptor type 2, phosphorylated 70-kd S6 protein kinase, 4E-binding protein 1, an...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325919</comments>
            <pubDate>Mon, 06 Jun 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325919</guid>        </item>
        <item>
            <title>Recent advances in the biology of Merkel cell carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5032288&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000785%2Fabstract%3Frss%3Dyes</link>
            <description>Summary: Recent outstanding research has rapidly revealed new aspects of the biology, etiology, and clinicopathology of Merkel cell carcinoma, a rare but highly aggressive neuroendocrine skin malignancy that affects the elderly and immunosuppressed patients. Molecular biological studies, especially the discovery of Merkel cell polyomavirus, have shed new light on the pathogenesis of the disease. Increasing evidence strongly suggests that this virus is causally related to the development of Merkel cell carcinoma. On the other hand, many studies have also indicated that a subset (approximately 20%) of Merkel cell carcinomas are not likely to be associated with the virus. Tumors with and without the virus have been shown to be significantly different in prognosis, oncogene expression, and his...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5032288</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5032288</guid>        </item>
        <item>
            <title>HER-2 discordance between primary gastric carcinoma and paired lymph node metastasis - reply</title>
            <link>http://www.medworm.com/index.php?rid=4834835&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000633%2Fabstract%3Frss%3Dyes</link>
            <description>In their letter to the editor, the authors describe an interesting case of a human epidermal growth factor receptor 2 (HER-2) negative primary gastric cancer with lymph node metastases containing an HER-2-amplified subpopulation making up 20% of the tumor cells in the lymph node. With this observation, the authors raised a highly important issue of heterogeneity of therapeutic targets and its potential impact on diagnostic procedures. Genetic heterogeneity is probably one of the most underestimated but critical issues in targeted therapy. For HER-2, the situation with respect to heterogeneity varies greatly between tumor types. Although HER-2 amplification is typically homogenous in breast and gastric cancer , there are other tumor types, such as bladder and colon cancer, where HER-2 ampli...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4834835</comments>
            <pubDate>Thu, 19 May 2011 14:50:31 +0100</pubDate>
            <guid isPermaLink="false">4834835</guid>        </item>
        <item>
            <title>HER-2 discordance between primary gastric carcinoma and paired lymph node metastasis</title>
            <link>http://www.medworm.com/index.php?rid=4834834&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711000621%2Fabstract%3Frss%3Dyes</link>
            <description>In their article published in the June 2009 issue of this journal, Marx et al evaluated HER-2 amplification and overexpression in a series of 166 primary gastric cancers and compared the results with those obtained on corresponding lymph node metastases. HER-2 amplification, assessed by fluorescence in situ hybridization (FISH), was found in 27 (16%) of the 166 primary tumors; and HER-2 overexpression, assessed by immunohistochemistry (IHC), in 32 (19%) of the 166 cases. Of the 69 paired lymph node metastases, 49 and 51 were evaluable by FISH and IHC, respectively. The HER-2 results were highly concordant with no evidence of discrepancy in FISH results between primary and matched metastasis. For IHC analysis, only 1 discordant case was seen. In addition, in their series, HER-2–positive c...</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4834834</comments>
            <pubDate>Thu, 19 May 2011 14:50:31 +0100</pubDate>
            <guid isPermaLink="false">4834834</guid>        </item>
        <item>
            <title>Introduction to the special education issue</title>
            <link>http://www.medworm.com/index.php?rid=4834815&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001171%2Fabstract%3Frss%3Dyes</link>
            <description>The national spotlight has been shining on medical education since 2010, the 100th anniversary of the Flexner report. That report changed undergraduate medical education dramatically and ushered in the era of postgraduate medical education. To mark the Flexner centennial, many recent conferences and symposia discussed new trends in medical education at both the undergraduate medical education and graduate medical education (GME) level. Attention to the medical education continuum from undergraduate medical education to GME to continuing medical education brought that important perspective to the forefront like never before. Thus, it is timely that this issue of Human Pathology examines different aspects of pathology education in 5 articles . (Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4834815</comments>
            <pubDate>Thu, 19 May 2011 14:50:24 +0100</pubDate>
            <guid isPermaLink="false">4834815</guid>        </item>
        <item>
            <title>In This Issue</title>
            <link>http://www.medworm.com/index.php?rid=4834814&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001705%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4834814</comments>
            <pubDate>Thu, 19 May 2011 14:50:24 +0100</pubDate>
            <guid isPermaLink="false">4834814</guid>        </item>
        <item>
            <title>Table of Contents</title>
            <link>http://www.medworm.com/index.php?rid=4834813&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001687%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4834813</comments>
            <pubDate>Thu, 19 May 2011 14:50:24 +0100</pubDate>
            <guid isPermaLink="false">4834813</guid>        </item>
        <item>
            <title>Information for Authors</title>
            <link>http://www.medworm.com/index.php?rid=4834812&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001699%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4834812</comments>
            <pubDate>Thu, 19 May 2011 14:50:24 +0100</pubDate>
            <guid isPermaLink="false">4834812</guid>        </item>
        <item>
            <title>Editorial Board</title>
            <link>http://www.medworm.com/index.php?rid=4834811&amp;cid=s_35623_32_f&amp;fid=35623&amp;url=http%3A%2F%2Fwww.humanpathol.com%2Farticle%2FPIIS0046817711001675%2Fabstract%3Frss%3Dyes</link>
            <description>(Source: Human Pathology)</description>
            <author>Human Pathology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4834811</comments>
            <pubDate>Thu, 19 May 2011 14:50:24 +0100</pubDate>
            <guid isPermaLink="false">4834811</guid>        </item>
    </channel>
</rss>

